Canonical Allele Identifier: PA2825179894
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1744511

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000539.2:p.Gln166Arg
CA276771986
NM_000548.5:c.497A>G