Canonical Allele Identifier: PA2828419577
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 373567
ClinVar RCV Id: RCV000413038 RCV003512037
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357334.1:p.Ser1109Arg
CA046905
NM_001370405.1:c.3325A>C
CA394288809
NM_001370405.1:c.3327T>A
CA394288819
NM_001370405.1:c.3327T>G