ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2826260273
Gene: SCN1A
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000417978
RCV001004732
ClinVar Variation:
381568
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Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001189364.1:p.Ile1638Asn
CA16603930
NM_001202435.3:c.4913T>A