Canonical Allele Identifier: PA2499231305
Gene: SCN4A HGNC NCBI

Linked Data

ClinVar Variation Id: 1028201
ClinVar RCV Id: RCV001329190
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000325.4:p.Phe1392Ser
CA400616560
NM_000334.4:c.4175T>C