Canonical Allele Identifier: PA916023013
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 141482
ClinVar RCV Id: RCV000130032 RCV001087672 RCV000836828 RCV003997543
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305760.1:p.Ala864Val
CA018885
NM_001318831.2:c.2591C>T