Canonical Allele Identifier: PA2828421667
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 65291
ClinVar RCV Id: RCV000055513 RCV001814036
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357334.1:p.Arg1696Leu
CA022229
NM_001370405.1:c.5087G>T