Canonical Allele Identifier: PA2828421187
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 838362

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357334.1:p.Met1572Arg
CA394308151
NM_001370405.1:c.4715T>G