Canonical Allele Identifier: PA263076
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 50016
ClinVar RCV Id: RCV000043284 RCV000695774
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000539.2:p.Asp1535Tyr
CA020751
NM_000548.5:c.4603G>T