Canonical Allele Identifier: PA2825940665
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67667
ClinVar RCV Id: RCV000058429 RCV000196670 RCV000239767 RCV000656174 RCV001842283
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153632.1:p.Arg523Cys
CA014976
NM_001160160.2:c.1567C>T