Canonical Allele Identifier: PA2825944867
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67847

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153633.1:p.Ile1280Val
CA017738
NM_001160161.2:c.3838A>G