Canonical Allele Identifier: PA2828094552
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 639390

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350457.1:p.Gln1459Arg
CA394304325
NM_001363528.2:c.4376A>G