Canonical Allele Identifier: PA2828420925
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2633616

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357334.1:p.Asp1498Gly
CA394304815
NM_001370405.1:c.4493A>G