Canonical Allele Identifier: PA2825945049
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67882

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153633.1:p.Ile1394Leu
CA018152
NM_001160161.2:c.4180A>C