Canonical Allele Identifier: PA262567
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 49310

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000539.2:p.Glu1552del
CA020824
NM_000548.5:c.4655_4657del