Canonical Allele Identifier: PA2825489622
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 1303356
ClinVar RCV Id: RCV001757911
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092874.1:p.Val1322Ala
CA352147649
NM_001099404.2:c.3965T>C