Canonical Allele Identifier: PA107707
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 12403

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000539.2:p.Arg905Gln
CA017951
NM_000548.5:c.2714G>A