Canonical Allele Identifier: PA210046
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 50148

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000539.2:p.Gly1204Glu
CA019384
NM_000548.5:c.3611G>A