Canonical Allele Identifier: PA2828095579
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 41747

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350457.1:p.Val1724Met
CA022424
NM_001363528.2:c.5170G>A