Canonical Allele Identifier: PA2827924129
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 3068546

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341630.1:p.Ile1949Val
CA064971
NM_001354701.2:c.5845A>G