Canonical Allele Identifier: PA2827007565
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 535981

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305758.1:p.Arg631Leu
CA394274563
NM_001318829.2:c.1892G>T