Canonical Allele Identifier: PA645435724
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 405943

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000539.2:p.Arg1745Cys
CA054522
NM_000548.5:c.5233C>T