Canonical Allele Identifier: PA2825491841
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 463358
ClinVar RCV Id: RCV000786216 RCV004545786 RCV003591749
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092875.1:p.Arg27Cys
CA056855
NM_001099405.2:c.79C>T