Allele Registry

Canonical Allele Identifier: PA2829981392

Gene: TSC2 HGNC NCBI

ClinVar RCV:

RCV000644143

RCV002331187

ClinVar Variation:

535914

HGVS (amino-acid)	Matching Registered Transcripts
NP_066399.2:p.Asn1445Ser	CA276753586 NM_021055.3:c.4334A>G