Allele Registry

Canonical Allele Identifier: PA101277

Gene: GSS HGNC NCBI

ClinVar RCV:

RCV003155734

ClinVar Variation:

2445815

HGVS (amino-acid)	Matching Registered Transcripts
NP_000169.1:p.Asp219Ala	CA408702823 NM_000178.2:c.656A>C