Canonical Allele Identifier: PA108698
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 68054

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_932173.1:p.Val294Met
CA019903
NM_198056.3:c.880G>A