Canonical Allele Identifier: PA2828093240
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 536003

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350457.1:p.Arg1084Gln
CA046441
NM_001363528.2:c.3251G>A