Canonical Allele Identifier: PA2828095402
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 65296
ClinVar RCV Id: RCV000055518

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350457.1:p.Leu1684Pro
CA022298
NM_001363528.2:c.5051T>C