Allele Registry

Canonical Allele Identifier: PA119695

Gene: GSS HGNC NCBI

ClinVar RCV:

RCV000009055

RCV003488332

ClinVar Variation:

8529

HGVS (amino-acid)	Matching Registered Transcripts
NP_000169.1:p.Arg125Cys	CA119694 NM_000178.2:c.373C>T