Canonical Allele Identifier: PA2825945865
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 2736875
ClinVar RCV Id: RCV003560108
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153633.1:p.Pro1905Arg
CA352139602
NM_001160161.2:c.5714C>G