Allele Registry

Canonical Allele Identifier: PA2827002281

Gene: TSC2 HGNC NCBI

ClinVar RCV:

RCV000055442

RCV002051805

ClinVar Variation:

65222

HGVS (amino-acid)	Matching Registered Transcripts
NP_001305756.1:p.Leu696Val	CA016903 NM_001318827.2:c.2086C>G