Canonical Allele Identifier: PA2828416761
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 50010
ClinVar RCV Id: RCV000043278 RCV000421501 RCV000457171 RCV001018037 RCV002262605
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357334.1:p.Met286Thr
CA023058
NM_001370405.1:c.857T>C