Canonical Allele Identifier: PA2825944922
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 1013702
ClinVar RCV Id: RCV003770639
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153633.1:p.Thr1313Pro
CA352146994
NM_001160161.2:c.3937A>C