Canonical Allele Identifier: PA2828406173
Gene: SIRT3 HGNC NCBI

Linked Data

ClinVar Variation Id: 2359125
ClinVar RCV Id: RCV004200838
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357250.1:p.Glu190Lys
CA378857855
NM_001370321.1:c.568G>A