Canonical Allele Identifier: PA2828411994
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 937500
ClinVar Variation Id: 1052187

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357333.1:p.Val679Leu
CA394274552
NM_001370404.1:c.2035G>C
CA394274554
NM_001370404.1:c.2035G>T