Canonical Allele Identifier: PA329932
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67765
ClinVar RCV Id: RCV000058535 RCV003539781 RCV002490654 RCV003996532
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Arg965Leu
CA016609
NM_000335.5:c.2894G>T