Canonical Allele Identifier: PA916036911
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68641
ClinVar RCV Id: RCV000059520 RCV003233101 RCV003588572
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340890.1:p.Arg834Cys
CA285189
NM_001353961.2:c.2500C>T