Canonical Allele Identifier: PA2827921225
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 1524249
ClinVar RCV Id: RCV003657669

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341630.1:p.Thr38Ala
CA352158816
NM_001354701.2:c.112A>G