Canonical Allele Identifier: PA2828421835
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1440541
ClinVar RCV Id: RCV001978883

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357334.1:p.Pro1734Thr
CA394315676
NM_001370405.1:c.5200C>A