Canonical Allele Identifier: PA2825941208
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67748
ClinVar RCV Id: RCV000183009 RCV000058517 RCV000619419 RCV000678939 RCV003996530
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153632.1:p.Arg893Cys
CA016390
NM_001160160.2:c.2677C>T