Canonical Allele Identifier: PA645453306
Gene: SCN4A HGNC NCBI

Linked Data

ClinVar Variation Id: 432825

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000325.4:p.Phe198Leu
CA400638901
NM_000334.4:c.594C>G
CA400638903
NM_000334.4:c.594C>A
CA400638910
NM_000334.4:c.592T>C