Canonical Allele Identifier: PA2827010938
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 535893

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305758.1:p.Tyr287Cys
CA027968
NM_001318829.2:c.860A>G