Allele Registry

Canonical Allele Identifier: PA2827877139

Gene: AHSG HGNC NCBI

ClinVar RCV:

RCV000017419

RCV001548865

ClinVar Variation:

16044

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341502.1:p.Ser228Thr	CA126165 NM_001354573.2:c.683G>C