Allele Registry

Canonical Allele Identifier: PA2827020959

Gene: TSC2 HGNC NCBI

ClinVar RCV:

RCV000043100

RCV001249601

ClinVar Variation:

49834

HGVS (amino-acid)	Matching Registered Transcripts
NP_001305761.1:p.Arg1687Gly	CA022207 NM_001318832.2:c.5059C>G