Canonical Allele Identifier: PA916023365
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 405959

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305761.1:p.Tyr360Cys
CA16614703
NM_001318832.2:c.1079A>G