Canonical Allele Identifier: PA218832
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67677
ClinVar RCV Id: RCV000058441 RCV001842290
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092874.1:p.Thr559Ile
CA015154
NM_001099404.2:c.1676C>T