Allele Registry

Canonical Allele Identifier: PA916023880

Gene: TSC2 HGNC NCBI

ClinVar RCV:

RCV000456253

RCV002451090

RCV004000723

ClinVar Variation:

406123

HGVS (amino-acid)	Matching Registered Transcripts
NP_001305761.1:p.Met799Ile	CA038757 NM_001318832.2:c.2397G>A CA394276962 NM_001318832.2:c.2397G>C CA394276964 NM_001318832.2:c.2397G>T