Allele Registry

Canonical Allele Identifier: PA2827005365

Gene: TSC2 HGNC NCBI

ClinVar RCV:

RCV000483888

ClinVar Variation:

421466

HGVS (amino-acid)	Matching Registered Transcripts
NP_001305756.1:p.Arg1610_Ala1613del	CA16620104 NM_001318827.2:c.4829_4840del