Allele Registry

Canonical Allele Identifier: PA2827008532

Gene: TSC2 HGNC NCBI

ClinVar RCV:

RCV000461553

RCV001019998

ClinVar Variation:

405981

HGVS (amino-acid)	Matching Registered Transcripts
NP_001305758.1:p.Ala1018Gly	CA16614990 NM_001318829.2:c.3053C>G