Canonical Allele Identifier: PA165564
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_000539.2:p.Ala1108Val
CA018885
NM_000548.5:c.3323C>T