Allele Registry

Canonical Allele Identifier: PA2827877059

Gene: AHSG HGNC NCBI

ClinVar RCV:

RCV004298770

ClinVar Variation:

2527438

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341500.1:p.Ala98Thr	CA2744824 NM_001354571.2:c.292G>A