Canonical Allele Identifier: PA645432465
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 318320

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000539.2:p.Thr771Ile
CA10637328
NM_000548.5:c.2312C>T