Canonical Allele Identifier: PA2826258200
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 265297
ClinVar RCV Id: RCV000255269 RCV000763462 RCV002521851
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001189364.1:p.Leu221Val
CA10588324
NM_001202435.3:c.661C>G