Allele Registry

Canonical Allele Identifier: PA916026666

Gene: GSS HGNC NCBI

ClinVar RCV:

RCV000009053

ClinVar Variation:

8527

HGVS (amino-acid)	Matching Registered Transcripts
NP_001309424.1:p.Arg267Trp	CA119692 NM_001322495.1:c.799C>T