Canonical Allele Identifier: PA1139690028
Gene: GSS HGNC NCBI

Linked Data

ClinVar Variation Id: 993915
ClinVar RCV Id: RCV001812966
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001309424.1:p.Lys306Glu
CA408701238
NM_001322495.1:c.916A>G