Allele Registry

Canonical Allele Identifier: PA2827016845

Gene: TSC2 HGNC NCBI

ClinVar Variation Id: 467968

HGVS (amino-acid)	Matching Registered Transcripts
NP_001305761.1:p.Arg104Trp	CA041936 NM_001318832.2:c.310C>T