Canonical Allele Identifier: PA2825084698
Gene: GSS HGNC NCBI

Linked Data

ClinVar Variation Id: 1163160
ClinVar RCV Id: RCV001507983
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000169.1:p.Pro272Leu
CA408702245
NM_000178.2:c.815C>T