Canonical Allele Identifier: PA2825438058
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 535925

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070651.1:p.Arg1262Cys
CA049839
NM_001077183.3:c.3784C>T