Allele Registry

Canonical Allele Identifier: PA2580223556

Gene: AHSG HGNC NCBI

ClinVar RCV:

RCV004207158

ClinVar Variation:

2367712

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341500.1:p.Pro360Leu	CA2745105 NM_001354571.2:c.1079C>T