Allele Registry

Canonical Allele Identifier: PA2828413638

Gene: TSC2 HGNC NCBI

ClinVar RCV:

RCV000042789

RCV000254034

RCV001069687

ClinVar Variation:

49529

HGVS (amino-acid)	Matching Registered Transcripts
NP_001357333.1:p.Trp1164Gly	CA019409 NM_001370404.1:c.3490T>G