Canonical Allele Identifier: PA2829977274
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 65074

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066399.2:p.Ala889Pro
CA017834
NM_021055.3:c.2665G>C