Canonical Allele Identifier: PA915976276
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 207738
ClinVar RCV Id: RCV000231299 RCV000561234 RCV001705073 RCV003996891
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107854.1:p.Thr996Ala
CA043628
NM_001114382.3:c.2986A>G