Canonical Allele Identifier: PA2741815541
Gene: SCN4A HGNC NCBI

Linked Data

ClinVar Variation Id: 2648086

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000325.4:p.Glu1607Lys
CA8708897
NM_000334.4:c.4819G>A