Canonical Allele Identifier: PA2828415879
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1741816
ClinVar RCV Id: RCV002342383

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357334.1:p.Phe15Leu
CA394300917
NM_001370405.1:c.43T>C
CA394300943
NM_001370405.1:c.45T>A
CA394300947
NM_001370405.1:c.45T>G