Canonical Allele Identifier: PA2825491619
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 3068546
ClinVar RCV Id: RCV003994615 RCV004006197
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092874.1:p.Ile1968Val
CA064971
NM_001099404.2:c.5902A>G