Canonical Allele Identifier: PA2580108919
Gene: SCN4A HGNC NCBI

Linked Data

ClinVar Variation Id: 1807333
ClinVar RCV Id: RCV002475290
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000325.4:p.Phe1494Tyr
CA400615934
NM_000334.4:c.4481T>A