Canonical Allele Identifier: PA658681168
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 468061

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000539.2:p.Arg1355Gly
CA394299372
NM_000548.5:c.4063A>G