Canonical Allele Identifier: PA264951
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67671
ClinVar RCV Id: RCV000058434 RCV000182979 RCV000490338 RCV001842287 RCV002483110
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Phe532Cys
CA015051
NM_000335.5:c.1595T>G