Canonical Allele Identifier: PA2825577612
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2119302
ClinVar RCV Id: RCV003054591

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107854.1:p.Ile1724_Arg1728delinsSer
CA2580091167
NM_001114382.3:c.5171_5182del