Canonical Allele Identifier: PA2828094934
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 207757

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350457.1:p.Arg1568Cys
CA053034
NM_001363528.2:c.4702C>T