Allele Registry

Canonical Allele Identifier: PA126166

Gene: AHSG HGNC NCBI

ClinVar RCV:

RCV000017419

RCV001548865

ClinVar Variation:

16044

HGVS (amino-acid)	Matching Registered Transcripts
NP_001613.2:p.Ser256Thr	CA126165 NM_001622.4:c.767G>C