Canonical Allele Identifier: PA2827777708
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 2707845
ClinVar RCV Id: RCV003589893
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340883.1:p.Leu1663Phe
CA349069648
NM_001353954.2:c.4987C>T