Allele Registry

Canonical Allele Identifier: PA2828420672

Gene: TSC2 HGNC NCBI

ClinVar RCV:

RCV000462201

RCV004000704

ClinVar Variation:

406035

HGVS (amino-acid)	Matching Registered Transcripts
NP_001357334.1:p.Arg1431Gly	CA051088 NM_001370405.1:c.4291A>G