Allele Registry

Canonical Allele Identifier: PA2827877096

Gene: AHSG HGNC NCBI

ClinVar RCV:

RCV000017419

RCV001548865

ClinVar Variation:

16044

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341501.1:p.Ser255Thr	CA126165 NM_001354572.2:c.764G>C