Canonical Allele Identifier: PA2580108147
Gene: SCN4A HGNC NCBI

Linked Data

ClinVar Variation Id: 2009973
ClinVar RCV Id: RCV002842823

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000325.4:p.Cys737Arg
CA400630188
NM_000334.4:c.2209T>C