Canonical Allele Identifier: PA2825943613
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67656

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153633.1:p.Glu446Lys
CA014706
NM_001160161.2:c.1336G>A