Canonical Allele Identifier: PA2827002665
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 391969

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305756.1:p.Thr812Ala
CA16607307
NM_001318827.2:c.2434A>G