Canonical Allele Identifier: PA2827005463
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 536037
ClinVar Variation Id: 825544

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305756.1:p.Asp1631Asn
CA054398
NM_001318827.2:c.4891G>A
CA915946265
NM_001318827.2:c.4891_4893delinsAAC