Canonical Allele Identifier: PA2828418766
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 185434
ClinVar RCV Id: RCV000164859 RCV000407000 RCV001086946
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357334.1:p.Ala862Thr
CA017691
NM_001370405.1:c.2584G>A