Canonical Allele Identifier: PA2827017346
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 238094

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305761.1:p.His289Arg
CA10583286
NM_001318832.2:c.866A>G