ClinGen Allele Registry
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Canonical Allele Identifier:
PA2827785292
Gene: SCN1A
HGNC
NCBI
Linked Data
ClinVar RCV:
RCV000059390
RCV002513779
ClinVar Variation:
68518
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001340887.1:p.Thr784Arg
CA284895
NM_001353958.2:c.2351C>G