Canonical Allele Identifier: PA658680415
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 480835

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000539.2:p.Tyr274Cys
CA394313259
NM_000548.5:c.821A>G