Canonical Allele Identifier: PA195504
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 186667

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000539.2:p.Arg718His
CA016838
NM_000548.5:c.2153G>A