Allele Registry

Canonical Allele Identifier: PA2829977368

Gene: TSC2 HGNC NCBI

ClinVar Variation Id: 207783

HGVS (amino-acid)	Matching Registered Transcripts
NP_066399.2:p.Arg901Cys	CA319592 NM_021055.3:c.2701C>T