Canonical Allele Identifier: PA2828095091
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 12393
ClinVar RCV Id: RCV000013201 RCV000043065 RCV000055436 RCV000493720 RCV002345240 RCV002496339
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350457.1:p.Pro1609Leu
CA021526
NM_001363528.2:c.4826C>T