ClinGen Allele Registry
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Canonical Allele Identifier:
PA2827755693
Gene: SCN1A
HGNC
NCBI
Linked Data
ClinVar RCV:
RCV000188919
RCV001241778
RCV002225093
RCV002485282
ClinVar Variation:
206802
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001340878.1:p.Arg28Cys
CA317371
NM_001353949.2:c.82C>T