Canonical Allele Identifier: PA2825944864
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67844

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153633.1:p.Pro1278Leu
CA017721
NM_001160161.2:c.3833C>T