Canonical Allele Identifier: PA658680843
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 467940

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000539.2:p.Arg799Cys
CA394277095
NM_000548.5:c.2395C>T