Allele Registry

Canonical Allele Identifier: PA2828410759

Gene: TSC2 HGNC NCBI

ClinVar RCV:

RCV000474153

ClinVar Variation:

406128

HGVS (amino-acid)	Matching Registered Transcripts
NP_001357333.1:p.Asn331Asp	CA16614698 NM_001370404.1:c.991A>G