Canonical Allele Identifier: PA2825940895
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67703
ClinVar RCV Id: RCV000058470 RCV003398647 RCV003541644
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153632.1:p.Arg661Trp
CA015679
NM_001160160.2:c.1981C>T