Canonical Allele Identifier: PA915960959
Gene: SCN4A HGNC NCBI

Linked Data

ClinVar Variation Id: 644159

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000325.4:p.Ala1636Val
CA292956782
NM_000334.4:c.4907C>T