Canonical Allele Identifier: PA2827012818
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1779692
ClinVar RCV Id: RCV002401747 RCV003512176
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305760.1:p.Met389Thr
CA394272876
NM_001318831.2:c.1166T>C