Canonical Allele Identifier: PA2827923158
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 1409689
ClinVar RCV Id: RCV003657448
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341630.1:p.Cys1340Arg
CA352147447
NM_001354701.2:c.4018T>C