ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA107535
Gene: SCN1A
HGNC
NCBI
Linked Data
ClinVar RCV:
RCV000059540
RCV000489760
RCV000764284
RCV000792317
ClinVar Variation:
68660
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001159435.1:p.Glu1795Lys
CA266126
NM_001165963.4:c.5383G>A