Canonical Allele Identifier: PA2827003844
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 951136

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305756.1:p.Arg1188Leu
CA394293592
NM_001318827.2:c.3563G>T