Canonical Allele Identifier: PA2825944870
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 3008823
ClinVar RCV Id: RCV003861950

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153633.1:p.Met1281Val
CA72944913
NM_001160161.2:c.3841A>G