Canonical Allele Identifier: PA2827016455
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 405943

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305760.1:p.Arg1501Cys
CA054522
NM_001318831.2:c.4501C>T