Canonical Allele Identifier: PA330147
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67933

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092874.1:p.Arg1623Leu
CA018677
NM_001099404.2:c.4868G>T