Canonical Allele Identifier: PA2573170652
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1478025

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000539.2:p.Ala1782Thr
CA394315690
NM_000548.5:c.5344G>A