Canonical Allele Identifier: PA2825942890
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 520462

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153632.1:p.Val1947Phe
CA065024
NM_001160160.2:c.5839G>T