Canonical Allele Identifier: PA2827787985
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 167646
ClinVar RCV Id: RCV000471353 RCV000515440 RCV000710209 RCV002408682
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340889.1:p.Arg579Gln
CA234868
NM_001353960.2:c.1736G>A