Canonical Allele Identifier: PA916021216
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_001299801.1:p.Thr64Pro
CA144003
NM_001312872.1:c.190A>C