Canonical Allele Identifier: PA2825573992
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 50189

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107854.1:p.Met649Thr
CA016283
NM_001114382.3:c.1946T>C