Canonical Allele Identifier: PA2828093058
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 406055
ClinVar RCV Id: RCV000457622 RCV002446790
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350457.1:p.Arg1035Gln
CA044900
NM_001363528.2:c.3104G>A