Allele Registry

Canonical Allele Identifier: PA2828405991

Gene: SIRT3 HGNC NCBI

ClinVar RCV:

RCV003973953

ClinVar Variation:

3057000

HGVS (amino-acid)	Matching Registered Transcripts
NP_001357243.1:p.Arg80Trp	CA5771286 NM_001370314.1:c.238C>T