Allele Registry

Canonical Allele Identifier: PA2825575782

Gene: TSC2 HGNC NCBI

ClinVar RCV:

RCV000042787

RCV000660346

ClinVar Variation:

49527

HGVS (amino-acid)	Matching Registered Transcripts
NP_001107854.1:p.Gly1204Arg	CA019365 NM_001114382.3:c.3610G>A CA394289756 NM_001114382.3:c.3610G>C