Canonical Allele Identifier: PA2827003019
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 649255

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305756.1:p.Ser919Thr
CA394283753
NM_001318827.2:c.2756G>C