Allele Registry

Canonical Allele Identifier: PA126164

Gene: AHSG HGNC NCBI

ClinVar RCV:

RCV000017418

RCV001548864

ClinVar Variation:

16043

HGVS (amino-acid)	Matching Registered Transcripts
NP_001613.2:p.Met248Thr	CA126163 NM_001622.4:c.743T>C