Canonical Allele Identifier: PA2825942622
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 936302
ClinVar RCV Id: RCV002348667 RCV003656462
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153632.1:p.Pro1791Leu
CA352141039
NM_001160160.2:c.5372C>T