Allele Registry

Canonical Allele Identifier: PA101249

Gene: GSS HGNC NCBI

ClinVar RCV:

RCV000009053

ClinVar Variation:

8527

HGVS (amino-acid)	Matching Registered Transcripts
NP_000169.1:p.Arg267Trp	CA119692 NM_000178.2:c.799C>T