Canonical Allele Identifier: PA2825132917
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_000326.2:p.Ala2001Thr
CA10576613
NM_000335.5:c.6001G>A