Canonical Allele Identifier: PA2825538783
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 406413

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092874.1:p.Arg1174Trp
CA061963
NM_001099404.2:c.3520C>T