Canonical Allele Identifier: PA915960976
Gene: SCN4A HGNC NCBI

Linked Data

ClinVar Variation Id: 654237
ClinVar RCV Id: RCV000810158
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000325.4:p.Glu1702Val
CA400614061
NM_000334.4:c.5105A>T