Canonical Allele Identifier: PA2827012534
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1056722

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305760.1:p.Thr309Ser
CA394326254
NM_001318831.2:c.925A>T
CA394326260
NM_001318831.2:c.926C>G