Canonical Allele Identifier: PA2825439596
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1505927

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070651.1:p.Arg1686Pro
CA394314815
NM_001077183.3:c.5057G>C