Allele Registry

Canonical Allele Identifier: PA210069

Gene: TSC2 HGNC NCBI

ClinVar RCV:

RCV000042990

RCV000189999

RCV000201105

ClinVar Variation:

49725

HGVS (amino-acid)	Matching Registered Transcripts
NP_000539.2:p.Cys804Arg	CA017384 NM_000548.5:c.2410T>C