Canonical Allele Identifier: PA218879
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67766
ClinVar RCV Id: RCV000058536 RCV001842320
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Arg971Cys
CA016616
NM_000335.5:c.2911C>T