Canonical Allele Identifier: PA2827004773
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1519233
ClinVar RCV Id: RCV002024455

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305756.1:p.Tyr1446His
CA394304973
NM_001318827.2:c.4336T>C