Allele Registry

Canonical Allele Identifier: PA2829981436

Gene: TSC2 HGNC NCBI

ClinVar Variation Id: 49490

HGVS (amino-acid)	Matching Registered Transcripts
NP_066399.2:p.Pro1454Thr	CA020509 NM_021055.3:c.4360C>A