Canonical Allele Identifier: PA2825944747
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 938518
ClinVar RCV Id: RCV003656486

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153633.1:p.Met1200Lys
CA352149167
NM_001160161.2:c.3599T>A