Canonical Allele Identifier: PA2827923534
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 1743377
ClinVar RCV Id: RCV002330764
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341630.1:p.Leu1589Arg
CA352143150
NM_001354701.2:c.4766T>G