Canonical Allele Identifier: PA2828092656
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 12403

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350457.1:p.Arg905Gln
CA017951
NM_001363528.2:c.2714G>A