Canonical Allele Identifier: PA2827020965
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 405943

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305761.1:p.Arg1689Cys
CA054522
NM_001318832.2:c.5065C>T