Allele Registry

Canonical Allele Identifier: PA2829981158

Gene: TSC2 HGNC NCBI

ClinVar Variation Id: 497137

HGVS (amino-acid)	Matching Registered Transcripts
NP_066399.2:p.Pro1415Thr	CA394301760 NM_021055.3:c.4243C>A