Allele Registry

Canonical Allele Identifier: PA658740715

Gene: AHSG HGNC NCBI

ClinVar RCV:

RCV000578120

ClinVar Variation:

488189

HGVS (amino-acid)	Matching Registered Transcripts
NP_001613.2:p.Arg317His	CA2745077 NM_001622.4:c.950G>A