Canonical Allele Identifier: PA2827770936
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 206805
ClinVar RCV Id: RCV000188922
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340880.1:p.His1206Arg
CA317383
NM_001353951.2:c.3617A>G