ClinGen Allele Registry
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Canonical Allele Identifier:
PA2825575800
Gene: TSC2
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000042789
RCV000254034
RCV001069687
ClinVar Variation:
49529
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001107854.1:p.Trp1208Gly
CA019409
NM_001114382.3:c.3622T>G