Canonical Allele Identifier: PA2825495434
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 201497

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092875.1:p.Arg1193Trp
CA017280
NM_001099405.2:c.3577C>T