Allele Registry

Canonical Allele Identifier: PA2827019860

Gene: TSC2 HGNC NCBI

ClinVar Variation Id: 406124

HGVS (amino-acid)	Matching Registered Transcripts
NP_001305761.1:p.Arg1395Cys	CA050953 NM_001318832.2:c.4183C>T