ClinGen Allele Registry
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Canonical Allele Identifier:
PA284993
Gene: SCN1A
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000059432
RCV000188986
RCV000763457
RCV001198988
RCV001208285
RCV002316217
ClinVar Variation:
68558
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_008851.3:p.Arg1634Gln
CA284991
NM_006920.6:c.4901G>A