Allele Registry

Canonical Allele Identifier: PA916037940

Gene: AHSG HGNC NCBI

ClinVar RCV:

RCV000017419

RCV001548865

ClinVar Variation:

16044

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341500.1:p.Ser257Thr	CA126165 NM_001354571.2:c.770G>C