Canonical Allele Identifier: PA2825491371
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 520459

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092874.1:p.Met1875dup
CA542615522
NM_001099404.2:c.5623_5625dup