Canonical Allele Identifier: PA2827005664
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 405968
ClinVar RCV Id: RCV000471005 RCV000562164 RCV000610568 RCV003392272 RCV004000682
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305756.1:p.Thr1677Ile
CA055164
NM_001318827.2:c.5030C>T