Protein level identifier (NP_000208):
p.Pro244His
cDNA level identifier (NM_000217):
c.731C>A
Gene level identifier:
g.2205C>A
Reference, alternative allele:
C, A
Genomic location hg(19)
12:5021275 (not available on ExAC)
Gene name:
Consequence:
missense
Pathogenicity scoring:
Probably pathogenic
CADD score:
31
Positive functional evidence:
not available
Number of all included cases:
2 heterozygous (2 in total).