Allele Registry

Canonical Allele Identifier: PA2827018611

Gene: TSC2 HGNC NCBI

ClinVar RCV:

RCV000467462

ClinVar Variation:

406049

HGVS (amino-acid)	Matching Registered Transcripts
NP_001305761.1:p.Thr1035Pro	CA16615089 NM_001318832.2:c.3103A>C