Canonical Allele Identifier: PA2825945726
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 520459

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153633.1:p.Met1821dup
CA542615522
NM_001160161.2:c.5461_5463dup