Allele Registry

Canonical Allele Identifier: PA2829335555

Gene: AHSG HGNC NCBI

ClinVar RCV:

RCV004242767

ClinVar Variation:

2411213

HGVS (amino-acid)	Matching Registered Transcripts
NP_001613.2:p.Val272Met	CA2745046 NM_001622.4:c.814G>A