Canonical Allele Identifier: PA2828410239
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1744511

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357333.1:p.Gln166Arg
CA276771986
NM_001370404.1:c.497A>G