Canonical Allele Identifier: PA263155
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 50114
ClinVar RCV Id: RCV000043381
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000539.2:p.Leu916Arg
CA018075
NM_000548.5:c.2747T>G