Canonical Allele Identifier: PA119691
Gene: GSS HGNC NCBI

Linked Data

ClinVar Variation Id: 8525
ClinVar RCV Id: RCV000009051 RCV001565039 RCV002512928
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000169.1:p.Arg164Gln
CA119690
NM_000178.2:c.491G>A