Canonical Allele Identifier: PA645432415
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 406077

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000539.2:p.Arg718Cys
CA036889
NM_000548.5:c.2152C>T