ClinGen Allele Registry
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Canonical Allele Identifier:
PA2827786058
Gene: SCN1A
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000180946
RCV001219498
RCV002272155
ClinVar Variation:
189990
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001340887.1:p.Leu1324Pro
CA303491
NM_001353958.2:c.3971T>C