Canonical Allele Identifier: PA181488
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67824
ClinVar RCV Id: RCV000058599 RCV000154838 RCV000620228 RCV001842349
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092874.1:p.Val1251Met
CA017494
NM_001099404.2:c.3751G>A