Canonical Allele Identifier: PA281755
Gene: SCN1A HGNC NCBI
ClinVar RCV:
RCV000022765
ClinVar Variation:
29884
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159435.1:p.Arg862Gly
CA281752
NM_001165963.4:c.2584C>G