Allele Registry

Canonical Allele Identifier: PA2827877158

Gene: AHSG HGNC NCBI

ClinVar RCV:

RCV004207158

ClinVar Variation:

2367712

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341502.1:p.Pro331Leu	CA2745105 NM_001354573.2:c.992C>T