Canonical Allele Identifier: PA645432359
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 226045

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000539.2:p.Val692Ile
CA036245
NM_000548.5:c.2074G>A