ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2828411405
Gene: TSC2
HGNC
NCBI
Linked Data
ClinVar Variation Id:
64901
ClinVar RCV Id:
RCV000055102
RCV003441735
RCV003512005
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Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001357333.1:p.Leu528Pro
CA015160
NM_001370404.1:c.1583T>C