Canonical Allele Identifier: PA2828415583
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 574061
ClinVar RCV Id: RCV000695896

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357333.1:p.Arg1707Pro
CA394314761
NM_001370404.1:c.5120G>C