Canonical Allele Identifier: PA2828092832
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1475211

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350457.1:p.Ser959Tyr
CA394283809
NM_001363528.2:c.2876C>A