Canonical Allele Identifier: PA2827923825
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 9377

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341630.1:p.Glu1765Lys
CA019148
NM_001354701.2:c.5293G>A