Canonical Allele Identifier: PA2829983446
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1745939

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066399.2:p.Pro1689Leu
CA394314204
NM_021055.3:c.5066C>T