Canonical Allele Identifier: PA098090
Gene: UQCC3 HGNC NCBI

Linked Data

ClinVar Variation Id: 161120
ClinVar RCV Id: RCV000148301
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001078841.1:p.Val20Glu
CA174000
NM_001085372.3:c.59T>A