Canonical Allele Identifier: PA2828413668
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1374125
ClinVar RCV Id: RCV001877669

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357333.1:p.Ser1177Thr
CA394292074
NM_001370404.1:c.3529T>A