Canonical Allele Identifier: PA916036897
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68557
ClinVar RCV Id: RCV000059431 RCV000176634 RCV000463147 RCV000623263 RCV002281560 RCV003448258
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340890.1:p.Arg822Gln
CA145253
NM_001353961.2:c.2465G>A