Allele Registry

Canonical Allele Identifier: PA2825576778

Gene: TSC2 HGNC NCBI

ClinVar RCV:

RCV000475369

RCV000574084

ClinVar Variation:

207755

HGVS (amino-acid)	Matching Registered Transcripts
NP_001107854.1:p.Ser1503Tyr	CA319534 NM_001114382.3:c.4508C>A