Canonical Allele Identifier: PA2828415569
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2119302
ClinVar RCV Id: RCV003054591

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357333.1:p.Ile1703_Arg1707delinsSer
CA2580091167
NM_001370404.1:c.5108_5119del