Canonical Allele Identifier: PA2825491825
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 48306
ClinVar RCV Id: RCV000041626 RCV000058779 RCV000766749 RCV001841609 RCV002345328
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092875.1:p.Arg18Gln
CA019208
NM_001099405.2:c.53G>A