Canonical Allele Identifier: PA2827012541
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 655069
ClinVar RCV Id: RCV000811171
ClinVar Variation Id: 1720529
ClinVar RCV Id: RCV002298256
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305760.1:p.Leu311Phe
CA031010
NM_001318831.2:c.933G>T
CA394326294
NM_001318831.2:c.933G>C