Canonical Allele Identifier: PA265084
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67732
ClinVar RCV Id: RCV000058501 RCV000497380 RCV000620361 RCV001258075 RCV000824760 RCV001842314 RCV003322595
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Arg814Gln
CA016182
NM_000335.5:c.2441G>A