Canonical Allele Identifier: PA2828420687
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1052237
ClinVar RCV Id: RCV001360380

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357334.1:p.Asp1435Ala
CA394302259
NM_001370405.1:c.4304A>C