Canonical Allele Identifier: PA2828093152
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 535906

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350457.1:p.Val1059Met
CA045672
NM_001363528.2:c.3175G>A