Allele Registry

Canonical Allele Identifier: PA2827877095

Gene: AHSG HGNC NCBI

ClinVar RCV:

RCV000017418

RCV001548864

ClinVar Variation:

16043

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341501.1:p.Met247Thr	CA126163 NM_001354572.2:c.740T>C