Canonical Allele Identifier: PA2825940352
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 984481
ClinVar RCV Id: RCV001264496
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153632.1:p.Leu308Val
CA352150338
NM_001160160.2:c.922C>G