Canonical Allele Identifier: PA2825942995
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67978

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153633.1:p.Arg18Trp
CA019099
NM_001160161.2:c.52C>T