Canonical Allele Identifier: PA2499233280
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1046768

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000539.2:p.Arg1529Leu
CA394304452
NM_000548.5:c.4586G>T