Canonical Allele Identifier: PA307552
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 201497
ClinVar RCV Id: RCV000183039 RCV000239165 RCV001842918 RCV002453661
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092874.1:p.Arg1193Trp
CA017280
NM_001099404.2:c.3577C>T