ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2828415522
Gene: TSC2
HGNC
NCBI
Linked Data
ClinVar Variation Id:
2416226
ClinVar RCV Id:
RCV003106975
RCV003384352
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Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001357333.1:p.Tyr1692Cys
CA394314314
NM_001370404.1:c.5075A>G