Canonical Allele Identifier: PA658804874
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 535920

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000539.2:p.Ile44Thr
CA394301782
NM_000548.5:c.131T>C