Canonical Allele Identifier: PA2827018984
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 535949

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305761.1:p.Ser1137Leu
CA394289260
NM_001318832.2:c.3410C>T