Allele Registry

Canonical Allele Identifier: PA916037939

Gene: AHSG HGNC NCBI

ClinVar RCV:

RCV000017418

RCV001548864

ClinVar Variation:

16043

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341500.1:p.Met249Thr	CA126163 NM_001354571.2:c.746T>C