Allele Registry

Canonical Allele Identifier: PA119697

Gene: GSS HGNC NCBI

ClinVar RCV:

RCV000009056

RCV000601337

RCV002227019

ClinVar Variation:

8530

HGVS (amino-acid)	Matching Registered Transcripts
NP_000169.1:p.Pro314Leu	CA119696 NM_000178.2:c.941C>T