Allele Registry

Canonical Allele Identifier: PA2825576974

Gene: TSC2 HGNC NCBI

ClinVar RCV:

RCV000043223

RCV002298454

ClinVar Variation:

49956

HGVS (amino-acid)	Matching Registered Transcripts
NP_001107854.1:p.Gly1556Ser	CA020963 NM_001114382.3:c.4666G>A