Allele Registry

Canonical Allele Identifier: PA2827877130

Gene: AHSG HGNC NCBI

ClinVar RCV:

RCV004246782

ClinVar Variation:

2410659

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341502.1:p.Val102Met	CA2744828 NM_001354573.2:c.304G>A