Canonical Allele Identifier: PA2580108432
Gene: SCN4A HGNC NCBI

Linked Data

ClinVar Variation Id: 1911420
ClinVar RCV Id: RCV002596939

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000325.4:p.Glu1210Lys
CA8709220
NM_000334.4:c.3628G>A