Allele Registry

Canonical Allele Identifier: PA2827877089

Gene: AHSG HGNC NCBI

ClinVar RCV:

RCV004257782

ClinVar Variation:

2462886

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341501.1:p.Asn178Ser	CA2744917 NM_001354572.2:c.533A>G