Canonical Allele Identifier: PA2828093540
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 535872

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350457.1:p.Pro1172Leu
CA276749978
NM_001363528.2:c.3515C>T