ClinGen Allele Registry
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Canonical Allele Identifier:
PA916036976
Gene: SCN1A
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000188995
RCV000781836
RCV001210054
RCV002336501
ClinVar Variation:
206861
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001340890.1:p.Asp926Asn
CA317589
NM_001353961.2:c.2776G>A