Allele Registry

Canonical Allele Identifier: PA2829983159

Gene: TSC2 HGNC NCBI

ClinVar Allele:

59091

ClinVar RCV:

RCV000043196

RCV000693889

ClinVar Variation:

49929

HGVS (amino-acid)	Matching Registered Transcripts
NP_066399.2:p.Pro1666Leu	CA021795 NM_021055.3:c.4997C>T