Canonical Allele Identifier: PA2825576779
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 49473
ClinVar Variation Id: 648504
ClinVar Variation Id: 2705118
ClinVar RCV Id: RCV003512908

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107854.1:p.Phe1504Leu
CA020719
NM_001114382.3:c.4510T>C
CA394304392
NM_001114382.3:c.4512T>A
CA394304402
NM_001114382.3:c.4512T>G