Canonical Allele Identifier: PA2825943838
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 2774478
ClinVar RCV Id: RCV003592360
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153633.1:p.Thr594Ile
CA352146184
NM_001160161.2:c.1781C>T