Canonical Allele Identifier: PA2828415716
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1440541
ClinVar RCV Id: RCV001978883

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357333.1:p.Pro1737Thr
CA394315676
NM_001370404.1:c.5209C>A