Canonical Allele Identifier: PA2828095535
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2840486
ClinVar RCV Id: RCV003628370

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350457.1:p.Thr1714Ala
CA394315648
NM_001363528.2:c.5140A>G