Canonical Allele Identifier: PA2827923479
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67918
ClinVar RCV Id: RCV000058699 RCV002336212 RCV003539784
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341630.1:p.Glu1555Lys
CA018503
NM_001354701.2:c.4663G>A