Allele Registry

Canonical Allele Identifier: PA2827168293

Gene: GSS HGNC NCBI

ClinVar RCV:

RCV003155734

ClinVar Variation:

2445815

HGVS (amino-acid)	Matching Registered Transcripts
NP_001309423.1:p.Asp219Ala	CA408702823 NM_001322494.1:c.656A>C