Allele Registry

Canonical Allele Identifier: PA2828411941

Gene: TSC2 HGNC NCBI

ClinVar RCV:

RCV000644337

RCV001013956

ClinVar Variation:

536057

HGVS (amino-acid)	Matching Registered Transcripts
NP_001357333.1:p.Pro665Ala	CA394274414 NM_001370404.1:c.1993C>G