Canonical Allele Identifier: PA2825944972
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67866

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153633.1:p.Val1351Met
CA017946
NM_001160161.2:c.4051G>A