Canonical Allele Identifier: PA645470790
Gene: GSS HGNC NCBI

Linked Data

ClinVar Variation Id: 338298

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000169.1:p.Met319Ile
CA9825925
NM_000178.2:c.957G>A
CA408701144
NM_000178.2:c.957G>T
CA408701145
NM_000178.2:c.957G>C