Canonical Allele Identifier: PA2827021000
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1505927

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305761.1:p.Arg1697Pro
CA394314815
NM_001318832.2:c.5090G>C