Canonical Allele Identifier: PA2825439716
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1440541
ClinVar RCV Id: RCV001978883

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070651.1:p.Pro1714Thr
CA394315676
NM_001077183.3:c.5140C>A