Canonical Allele Identifier: PA2825497186
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 9389
ClinVar RCV Id: RCV000009987 RCV000058786 RCV000154827 RCV000148848 RCV000619902 RCV000766811 RCV001841236 RCV002476953
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092875.1:p.Arg1808His
CA019280
NM_001099405.2:c.5423G>A