Canonical Allele Identifier: PA645432550
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 237994

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000539.2:p.Val841Ile
CA10583310
NM_000548.5:c.2521G>A