Canonical Allele Identifier: PA2825435860
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 49175

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070651.1:p.Tyr598His
CA015786
NM_001077183.3:c.1792T>C