Allele Registry

Canonical Allele Identifier: PA262846

Gene: TSC2 HGNC NCBI

ClinVar RCV:

RCV000042935

RCV002513627

ClinVar Variation:

49673

HGVS (amino-acid)	Matching Registered Transcripts
NP_000539.2:p.Arg381Lys	CA013922 NM_000548.5:c.1142G>A