Allele Registry

Canonical Allele Identifier: PA2828093180

Gene: TSC2 HGNC NCBI

ClinVar RCV:

RCV000461553

RCV001019998

ClinVar Variation:

405981

HGVS (amino-acid)	Matching Registered Transcripts
NP_001350457.1:p.Ala1067Gly	CA16614990 NM_001363528.2:c.3200C>G