Canonical Allele Identifier: PA2827011670
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 238097

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305760.1:p.Tyr110Cys
CA10583288
NM_001318831.2:c.329A>G