Canonical Allele Identifier: PA2828420883
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1741666
ClinVar RCV Id: RCV002342233

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357334.1:p.Arg1486Gly
CA394304450
NM_001370405.1:c.4456C>G