Canonical Allele Identifier: PA2829983685
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 65296
ClinVar RCV Id: RCV000055518

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066399.2:p.Leu1707Pro
CA022298
NM_021055.3:c.5120T>C