Canonical Allele Identifier: PA2825439595
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2814113
ClinVar RCV Id: RCV003627868

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070651.1:p.Arg1686Gly
CA394314811
NM_001077183.3:c.5056C>G