Canonical Allele Identifier: PA2828095407
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 574061
ClinVar RCV Id: RCV000695896

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350457.1:p.Arg1685Pro
CA394314761
NM_001363528.2:c.5054G>C