Allele Registry

Canonical Allele Identifier: PA101258

Gene: GSS HGNC NCBI

ClinVar RCV:

RCV000009054

RCV003488331

ClinVar Variation:

8528

HGVS (amino-acid)	Matching Registered Transcripts
NP_000169.1:p.Arg283Cys	CA119693 NM_000178.2:c.847C>T