Allele Registry

Canonical Allele Identifier: PA916026658

Gene: GSS HGNC NCBI

ClinVar RCV:

RCV000009055

RCV003488332

ClinVar Variation:

8529

HGVS (amino-acid)	Matching Registered Transcripts
NP_001309424.1:p.Arg125Cys	CA119694 NM_001322495.1:c.373C>T