Canonical Allele Identifier: PA2827921772
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 30048

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341630.1:p.Glu428Lys
CA014651
NM_001354701.2:c.1282G>A