Canonical Allele Identifier: PA2580203452
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1741816
ClinVar RCV Id: RCV002342383

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305761.1:p.Phe26Leu
CA394300917
NM_001318832.2:c.76T>C
CA394300943
NM_001318832.2:c.78T>A
CA394300947
NM_001318832.2:c.78T>G