Canonical Allele Identifier: PA2829977284
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 536006

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066399.2:p.His890Tyr
CA040850
NM_021055.3:c.2668C>T