Canonical Allele Identifier: PA2827011036
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2416226

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305758.1:p.Tyr1621Cys
CA394314314
NM_001318829.2:c.4862A>G