ClinGen Allele Registry
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Canonical Allele Identifier:
PA2826259879
Gene: SCN1A
HGNC
NCBI
Linked Data
ClinVar RCV:
RCV000059412
RCV002513780
ClinVar Variation:
68538
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001189364.1:p.Cys1396Gly
CA284943
NM_001202435.3:c.4186T>G