Canonical Allele Identifier: PA2825491858
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 201428
ClinVar RCV Id: RCV000182921 RCV001043149 RCV002500541 RCV003996807 RCV004546451
ClinVar Variation Id: 242209
ClinVar RCV Id: RCV000249341 RCV001722268 RCV001843010 RCV002500827 RCV004532970
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092875.1:p.Ala29Val
CA019870
NM_001099405.2:c.86_87delinsTG
CA019875
NM_001099405.2:c.86C>T