Canonical Allele Identifier: PA2827013961
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2092647
ClinVar RCV Id: RCV003008263

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305760.1:p.Lys706Glu
CA394279500
NM_001318831.2:c.2116A>G