Canonical Allele Identifier: PA218856
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67690
ClinVar RCV Id: RCV000058454
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092874.1:p.Val601Ala
CA015370
NM_001099404.2:c.1802T>C