ClinGen Allele Registry
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Canonical Allele Identifier:
PA2827782389
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_001340886.1:p.Arg837Gln
CA16042360
NM_001353957.2:c.2510G>A