Canonical Allele Identifier: PA2825491702
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 229236
ClinVar RCV Id: RCV000219261 RCV000766281 RCV002354612 RCV002500715 RCV001842985
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092874.1:p.Ala2002Thr
CA10576613
NM_001099404.2:c.6004G>A