Allele Registry

Canonical Allele Identifier: PA2829974918

Gene: TSC2 HGNC NCBI

ClinVar Variation Id: 405983

HGVS (amino-acid)	Matching Registered Transcripts
NP_066399.2:p.Lys657Gln	CA035326 NM_021055.3:c.1969A>C