Canonical Allele Identifier: PA2828418088
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2825177

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357334.1:p.Pro669Thr
CA394274455
NM_001370405.1:c.2005C>A