Canonical Allele Identifier: PA2827015689
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1047812
ClinVar RCV Id: RCV001352578

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305760.1:p.Thr1298Asn
CA394304832
NM_001318831.2:c.3893C>A