Allele Registry

Canonical Allele Identifier: PA2829978619

Gene: TSC2 HGNC NCBI

ClinVar RCV:

RCV000461553

RCV001019998

ClinVar Variation:

405981

HGVS (amino-acid)	Matching Registered Transcripts
NP_066399.2:p.Ala1067Gly	CA16614990 NM_021055.3:c.3200C>G