ClinGen Allele Registry
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Canonical Allele Identifier:
PA2826259092
Gene: SCN1A
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000413258
RCV000696398
RCV002248644
ClinVar Variation:
372566
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001189364.1:p.Arg865Gln
CA16042360
NM_001202435.3:c.2594G>A