Canonical Allele Identifier: PA265198
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67759
ClinVar RCV Id: RCV000058529
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Leu935Pro
CA016529
NM_000335.5:c.2804T>C