Canonical Allele Identifier: PA2825494381
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67730

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092875.1:p.Arg808Pro
CA016130
NM_001099405.2:c.2423G>C