Allele Registry

Canonical Allele Identifier: PA2829979338

Gene: TSC2 HGNC NCBI

ClinVar RCV:

RCV000469044

RCV001020619

RCV001721231

ClinVar Variation:

207678

HGVS (amino-acid)	Matching Registered Transcripts
NP_066399.2:p.Leu1146Val	CA319374 NM_021055.3:c.3436C>G