Canonical Allele Identifier: PA2825128851
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 960705
ClinVar RCV Id: RCV003656705
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Leu306Ile
CA352150351
NM_000335.5:c.916C>A