Canonical Allele Identifier: PA2825944655
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 201497

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153633.1:p.Arg1139Trp
CA017280
NM_001160161.2:c.3415C>T