Canonical Allele Identifier: PA2828415709
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2840486
ClinVar RCV Id: RCV003628370

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357333.1:p.Thr1736Ala
CA394315648
NM_001370404.1:c.5206A>G