Canonical Allele Identifier: PA2827004422
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 535870

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305756.1:p.Arg1354Trp
CA051001
NM_001318827.2:c.4060C>T