Allele Registry

Canonical Allele Identifier: PA916037942

Gene: AHSG HGNC NCBI

ClinVar RCV:

RCV000578120

ClinVar Variation:

488189

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341500.1:p.Arg318His	CA2745077 NM_001354571.2:c.953G>A