Canonical Allele Identifier: PA351468
Gene: COX20 HGNC NCBI

Linked Data

ClinVar Variation Id: 55889
ClinVar RCV Id: RCV000049300
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001299800.1:p.Thr52Pro
CA144003
NM_001312871.1:c.154A>C