Canonical Allele Identifier: PA2825491444
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 919315

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092874.1:p.Met1906Val
CA72937834
NM_001099404.2:c.5716A>G