Allele Registry

Canonical Allele Identifier: PA319351

Gene: TSC2 HGNC NCBI

ClinVar RCV:

RCV000189889

RCV000557687

RCV000564968

RCV000768351

RCV001200210

ClinVar Variation:

207659

HGVS (amino-acid)	Matching Registered Transcripts
NP_000539.2:p.Ser526Thr	CA031106 NM_000548.5:c.1577G>C