Allele Registry

Canonical Allele Identifier: PA2829972455

Gene: TSC2 HGNC NCBI

ClinVar Variation Id: 64956

HGVS (amino-acid)	Matching Registered Transcripts
NP_066399.2:p.Lys347Arg	CA013642 NM_021055.3:c.1040A>G