Allele Registry

Canonical Allele Identifier: PA916004571

Gene: SIRT1 HGNC NCBI

ClinVar RCV:

RCV000938820

RCV003925827

ClinVar Variation:

760832

HGVS (amino-acid)	Matching Registered Transcripts
NP_036370.2:p.His170Arg	CA5521028 NM_012238.5:c.509A>G