Allele Registry

Canonical Allele Identifier: PA101286

Gene: GSS HGNC NCBI

ClinVar RCV:

RCV000009057

RCV000984989

ClinVar Variation:

8531

HGVS (amino-acid)	Matching Registered Transcripts
NP_000169.1:p.Asp219Gly	CA119698 NM_000178.2:c.656A>G