Canonical Allele Identifier: PA2825489466
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 3075364
ClinVar RCV Id: RCV004016882
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092874.1:p.Val1284Ala
CA352148273
NM_001099404.2:c.3851T>C