Allele Registry

Canonical Allele Identifier: PA2827877100

Gene: AHSG HGNC NCBI

ClinVar RCV:

RCV004242767

ClinVar Variation:

2411213

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341501.1:p.Val271Met	CA2745046 NM_001354572.2:c.811G>A