Canonical Allele Identifier: PA2828093045
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3073959
ClinVar RCV Id: RCV004012501

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350457.1:p.Thr1032Pro
CA394285967
NM_001363528.2:c.3094A>C