Canonical Allele Identifier: PA2825437202
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 49566
ClinVar RCV Id: RCV000042826

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070651.1:p.Trp1016Arg
CA018659
NM_001077183.3:c.3046T>C
CA394285514
NM_001077183.3:c.3046T>A