Canonical Allele Identifier: PA2825574849
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 536006

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107854.1:p.His890Tyr
CA040850
NM_001114382.3:c.2668C>T