ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2827292755
Gene: SCN8A
HGNC
NCBI
Linked Data
ClinVar Variation Id:
207130
ClinVar RCV Id:
RCV000189288
RCV000792213
RCV004528970
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001317189.1:p.Thr1852Ile
CA318298
NM_001330260.2:c.5555C>T