Canonical Allele Identifier: PA2827922128
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67702

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341630.1:p.Glu654Lys
CA015639
NM_001354701.2:c.1960G>A