Allele Registry

Canonical Allele Identifier: PA2827877105

Gene: AHSG HGNC NCBI

ClinVar RCV:

RCV000578120

ClinVar Variation:

488189

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341501.1:p.Arg316His	CA2745077 NM_001354572.2:c.947G>A