Allele Registry

Canonical Allele Identifier: PA645390254

Gene: HGSNAT HGNC NCBI

ClinVar RCV:

RCV000488421

ClinVar Variation:

425553

HGVS (amino-acid)	Matching Registered Transcripts
NP_689632.2:p.Asp279Ala	CA371116505 NM_152419.3:c.836A>C