ClinGen Allele Registry
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Canonical Allele Identifier:
PA2826259660
Gene: SCN1A
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000013751
RCV000059501
RCV002513023
ClinVar Variation:
12891
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001189364.1:p.Lys1270Thr
CA256602
NM_001202435.3:c.3809A>C