Allele Registry

Canonical Allele Identifier: PA916023647

Gene: TSC2 HGNC NCBI

ClinVar RCV:

RCV000189988

RCV001236049

ClinVar Variation:

207722

HGVS (amino-acid)	Matching Registered Transcripts
NP_001305761.1:p.Lys610Arg	CA033543 NM_001318832.2:c.1829A>G