Canonical Allele Identifier: PA2827005522
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2119302
ClinVar RCV Id: RCV003054591

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305756.1:p.Ile1644_Arg1648delinsSer
CA2580091167
NM_001318827.2:c.4931_4942del