Canonical Allele Identifier: PA916022836
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 406049
ClinVar RCV Id: RCV000467462
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305756.1:p.Thr988Pro
CA16615089
NM_001318827.2:c.2962A>C