Canonical Allele Identifier: PA2828421686
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2119302
ClinVar RCV Id: RCV003054591

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357334.1:p.Ile1700_Arg1704delinsSer
CA2580091167
NM_001370405.1:c.5099_5110del