Allele Registry

Canonical Allele Identifier: PA2827008637

Gene: TSC2 HGNC NCBI

ClinVar RCV:

RCV000190077

RCV000644198

RCV002453704

ClinVar Variation:

207784

HGVS (amino-acid)	Matching Registered Transcripts
NP_001305758.1:p.Leu1050Pro	CA319595 NM_001318829.2:c.3149T>C