Canonical Allele Identifier: PA2827787939
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 206770
ClinVar RCV Id: RCV000188874 RCV001857646 RCV000585879 RCV002399702
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340889.1:p.Arg534His
CA317245
NM_001353960.2:c.1601G>A