Allele Registry

Canonical Allele Identifier: PA2829335579

Gene: AHSG HGNC NCBI

ClinVar RCV:

RCV004207158

ClinVar Variation:

2367712

HGVS (amino-acid)	Matching Registered Transcripts
NP_001613.2:p.Pro359Leu	CA2745105 NM_001622.4:c.1076C>T