Canonical Allele Identifier: PA317556
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 206852
ClinVar RCV Id: RCV000188984 RCV001244268
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159435.1:p.Arg1639Pro
CA317553
NM_001165963.4:c.4916G>C