Canonical Allele Identifier: PA2825435827
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1779692

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070651.1:p.Met589Thr
CA394272876
NM_001077183.3:c.1766T>C