Canonical Allele Identifier: PA2825439572
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2119302
ClinVar RCV Id: RCV003054591

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070651.1:p.Ile1680_Arg1684delinsSer
CA2580091167
NM_001077183.3:c.5039_5050del