Allele Registry

Canonical Allele Identifier: PA916023575

Gene: TSC2 HGNC NCBI

ClinVar Variation Id: 406036

HGVS (amino-acid)	Matching Registered Transcripts
NP_001305761.1:p.Pro554Ser	CA16615046 NM_001318832.2:c.1660C>T