Canonical Allele Identifier: PA2827921639
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67626
ClinVar RCV Id: RCV000058382 RCV000991046 RCV001841767 RCV001723640 RCV002362694 RCV002504968
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341630.1:p.Arg340Gln
CA014177
NM_001354701.2:c.1019G>A