Canonical Allele Identifier: PA2825497629
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 3068546

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092875.1:p.Ile1950Val
CA064971
NM_001099405.2:c.5848A>G