Canonical Allele Identifier: PA2827921494
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 68039

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341630.1:p.Val240Met
CA019765
NM_001354701.2:c.718G>A