Canonical Allele Identifier: PA658805023
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 535981

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000539.2:p.Arg680Leu
CA394274563
NM_000548.5:c.2039G>T