Canonical Allele Identifier: PA2828092831
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 229369

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350457.1:p.Gly958Glu
CA043736
NM_001363528.2:c.2873G>A