Canonical Allele Identifier: PA2827787660
Gene: SCN1A HGNC NCBI
ClinVar RCV:
RCV000258942
ClinVar Variation:
279592
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340889.1:p.Ala342Glu
CA10602709
NM_001353960.2:c.1025C>A