Allele Registry

Canonical Allele Identifier: PA2825573606

Gene: TSC2 HGNC NCBI

ClinVar RCV:

RCV000542715

RCV002395406

RCV003314613

ClinVar Variation:

467887

HGVS (amino-acid)	Matching Registered Transcripts
NP_001107854.1:p.Asp549Gly	CA394267934 NM_001114382.3:c.1646A>G