ClinGen Allele Registry
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Canonical Allele Identifier:
PA2828361657
Gene: SCN8A
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000636407
RCV000726306
RCV001197747
RCV002317158
ClinVar Variation:
207136
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001356717.1:p.Arg1919Gln
CA318309
NM_001369788.1:c.5756G>A