Canonical Allele Identifier: PA2741815546
Gene: SCN4A HGNC NCBI

Linked Data

ClinVar Variation Id: 2797364
ClinVar RCV Id: RCV003616132

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000325.4:p.Ala1636Thr
CA8708877
NM_000334.4:c.4906G>A