Canonical Allele Identifier: PA2827016411
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 536037
ClinVar Variation Id: 825544

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305760.1:p.Asp1490Asn
CA054398
NM_001318831.2:c.4468G>A
CA915946265
NM_001318831.2:c.4468_4470delinsAAC