Allele Registry

Canonical Allele Identifier: PA2827006927

Gene: TSC2 HGNC NCBI

ClinVar RCV:

RCV001011553

ClinVar Variation:

819200

HGVS (amino-acid)	Matching Registered Transcripts
NP_001305758.1:p.Gln429Glu	CA394324088 NM_001318829.2:c.1285C>G