Canonical Allele Identifier: PA2825490509
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 2505148
ClinVar RCV Id: RCV003233328
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092874.1:p.Ile1593Thr
CA352143636
NM_001099404.2:c.4778T>C