Canonical Allele Identifier: PA916022826
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 49566
ClinVar RCV Id: RCV000042826
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305756.1:p.Trp980Arg
CA018659
NM_001318827.2:c.2938T>C
CA394285514
NM_001318827.2:c.2938T>A