Canonical Allele Identifier: PA249090
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 50189

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000539.2:p.Met649Thr
CA016283
NM_000548.5:c.1946T>C