Canonical Allele Identifier: PA2828412940
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 839746

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357333.1:p.Gly957Val
CA043753
NM_001370404.1:c.2870G>T