Canonical Allele Identifier: PA2825189175
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3232189
ClinVar RCV Id: RCV004520872

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000539.2:p.His1746Tyr
CA394314606
NM_000548.5:c.5236C>T