Canonical Allele Identifier: PA2829983651
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2119302
ClinVar RCV Id: RCV003054591

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066399.2:p.Ile1704_Arg1708delinsSer
CA2580091167
NM_021055.3:c.5111_5122del