Allele Registry

Canonical Allele Identifier: PA645435590

Gene: TSC2 HGNC NCBI

ClinVar RCV:

RCV000483888

ClinVar Variation:

421466

HGVS (amino-acid)	Matching Registered Transcripts
NP_000539.2:p.Arg1713_Ala1716del	CA16620104 NM_000548.5:c.5138_5149del