Allele Registry

Canonical Allele Identifier: PA2825435026

Gene: TSC2 HGNC NCBI

ClinVar RCV:

RCV000474153

ClinVar Variation:

406128

HGVS (amino-acid)	Matching Registered Transcripts
NP_001070651.1:p.Asn331Asp	CA16614698 NM_001077183.3:c.991A>G