Canonical Allele Identifier: PA658681062
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 468020

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000539.2:p.Pro1176Ser
CA394289363
NM_000548.5:c.3526C>T