Canonical Allele Identifier: PA2827011317
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 937500
ClinVar Variation Id: 1052187

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305758.1:p.Val630Leu
CA394274552
NM_001318829.2:c.1888G>C
CA394274554
NM_001318829.2:c.1888G>T