Canonical Allele Identifier: PA2825494709
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 3069532
ClinVar RCV Id: RCV004008076
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092875.1:p.Leu947Phe
CA352140591
NM_001099405.2:c.2839C>T