Canonical Allele Identifier: PA264700
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 65304

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000539.2:p.Ser1498Thr
CA020540
NM_000548.5:c.4493G>C