Canonical Allele Identifier: PA2827009866
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 535895

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305758.1:p.Ala1445Thr
CA052272
NM_001318829.2:c.4333G>A