Allele Registry

Canonical Allele Identifier: PA2829335544

Gene: AHSG HGNC NCBI

ClinVar RCV:

RCV004257782

ClinVar Variation:

2462886

HGVS (amino-acid)	Matching Registered Transcripts
NP_001613.2:p.Asn179Ser	CA2744917 NM_001622.4:c.536A>G