Allele Registry

Canonical Allele Identifier: PA2829981100

Gene: TSC2 HGNC NCBI

ClinVar Variation Id: 406124

HGVS (amino-acid)	Matching Registered Transcripts
NP_066399.2:p.Arg1408Cys	CA050953 NM_021055.3:c.4222C>T