Canonical Allele Identifier: PA2825941942
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 201505

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153632.1:p.Ala1356Val
CA017845
NM_001160160.2:c.4067C>T