Allele Registry

Canonical Allele Identifier: PA2828082097

Gene: HGSNAT HGNC NCBI

ClinVar RCV:

RCV000488421

ClinVar Variation:

425553

HGVS (amino-acid)	Matching Registered Transcripts
NP_001350156.1:p.Asp279Ala	CA371116505 NM_001363227.2:c.836A>C