Canonical Allele Identifier: PA2825942711
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 520459

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153632.1:p.Met1842dup
CA542615522
NM_001160160.2:c.5524_5526dup