Allele Registry

Canonical Allele Identifier: PA2827877116

Gene: AHSG HGNC NCBI

ClinVar RCV:

RCV004207158

ClinVar Variation:

2367712

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341501.1:p.Pro358Leu	CA2745105 NM_001354572.2:c.1073C>T