Canonical Allele Identifier: PA2825942904
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 68020

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153632.1:p.Leu1955Arg
CA019559
NM_001160160.2:c.5864T>G