Allele Registry

Canonical Allele Identifier: PA2825439551

Gene: TSC2 HGNC NCBI

ClinVar RCV:

RCV000043100

RCV001249601

ClinVar Variation:

49834

HGVS (amino-acid)	Matching Registered Transcripts
NP_001070651.1:p.Arg1676Gly	CA022207 NM_001077183.3:c.5026C>G