Canonical Allele Identifier: PA2825942870
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 3068546

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153632.1:p.Ile1935Val
CA064971
NM_001160160.2:c.5803A>G