ClinGen Allele Registry
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Canonical Allele Identifier:
PA2828411335
Gene: TSC2
HGNC
NCBI
Linked Data
ClinVar RCV:
RCV000055200
RCV000688733
RCV001011980
RCV001085948
ClinVar Variation:
64996
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001357333.1:p.Arg505Gln
CA015034
NM_001370404.1:c.1514G>A