Canonical Allele Identifier: PA2828421698
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 65296
ClinVar RCV Id: RCV000055518

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357334.1:p.Leu1703Pro
CA022298
NM_001370405.1:c.5108T>C