Canonical Allele Identifier: PA2828095406
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 207760

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350457.1:p.Arg1685His
CA054581
NM_001363528.2:c.5054G>A