Allele Registry

Canonical Allele Identifier: PA2829981017

Gene: TSC2 HGNC NCBI

ClinVar RCV:

RCV001367751

ClinVar Variation:

1058594

HGVS (amino-acid)	Matching Registered Transcripts
NP_066399.2:p.Gly1400Val	CA394301384 NM_021055.3:c.4199G>T