Canonical Allele Identifier: PA2827790033
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1989927
ClinVar RCV Id: RCV002786755
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340889.1:p.His1900Arg
CA349063883
NM_001353960.2:c.5699A>G