Canonical Allele Identifier: PA2741815317
Gene: SCN4A HGNC NCBI

Linked Data

ClinVar Variation Id: 2800024
ClinVar RCV Id: RCV003616157

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000325.4:p.Val1179Ile
CA400618201
NM_000334.4:c.3535G>A