Allele Registry

Canonical Allele Identifier: PA2580223543

Gene: AHSG HGNC NCBI

ClinVar RCV:

RCV004257782

ClinVar Variation:

2462886

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341500.1:p.Asn180Ser	CA2744917 NM_001354571.2:c.539A>G