Canonical Allele Identifier: PA2827923972
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 520459

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341630.1:p.Met1856dup
CA542615522
NM_001354701.2:c.5566_5568dup