Canonical Allele Identifier: PA2827015637
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 848503

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305760.1:p.Glu1284Gln
CA394304419
NM_001318831.2:c.3850G>C