Canonical Allele Identifier: PA2827005667
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 238085

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305756.1:p.Pro1678Leu
CA10583347
NM_001318827.2:c.5033C>T