Allele Registry

Canonical Allele Identifier: PA2827021201

Gene: TSC2 HGNC NCBI

ClinVar RCV:

RCV000189951

RCV000696799

RCV002345683

ClinVar Variation:

207696

HGVS (amino-acid)	Matching Registered Transcripts
NP_001305761.1:p.Ile1741Leu	CA319402 NM_001318832.2:c.5221A>C