Canonical Allele Identifier: PA2825497503
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 179372
ClinVar RCV Id: RCV000156161 RCV000621933 RCV000765731 RCV002223795 RCV001842490
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092875.1:p.Arg1911His
CA019464
NM_001099405.2:c.5732G>A