Allele Registry

Canonical Allele Identifier: PA2580223548

Gene: AHSG HGNC NCBI

ClinVar RCV:

RCV004242767

ClinVar Variation:

2411213

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341500.1:p.Val273Met	CA2745046 NM_001354571.2:c.817G>A