Canonical Allele Identifier: PA2827020976
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2119302
ClinVar RCV Id: RCV003054591

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305761.1:p.Ile1691_Arg1695delinsSer
CA2580091167
NM_001318832.2:c.5072_5083del