Canonical Allele Identifier: PA2825132839
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 3068546

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Ile1967Val
CA064971
NM_000335.5:c.5899A>G