ClinGen Allele Registry
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Canonical Allele Identifier:
PA2825357888
Gene: SCN2A
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000013735
RCV001048768
RCV002284354
RCV002319419
RCV002513021
ClinVar Variation:
12875
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001035233.1:p.Arg188Trp
CA122767
NM_001040143.2:c.562C>T