Canonical Allele Identifier: PA2825945536
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67974

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153633.1:p.Val1709Met
CA019062
NM_001160161.2:c.5125G>A