Allele Registry

Canonical Allele Identifier: PA2827003387

Gene: TSC2 HGNC NCBI

ClinVar RCV:

RCV004520826

ClinVar Variation:

3232143

HGVS (amino-acid)	Matching Registered Transcripts
NP_001305756.1:p.Ser1052Trp	CA394286828 NM_001318827.2:c.3155C>G