Canonical Allele Identifier: PA2741984891
Gene: CCDC86 HGNC NCBI
ClinVar RCV:
RCV004320576
ClinVar Variation:
2543613
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077003.1:p.Ala149Gly
CA6026714
NM_024098.4:c.446C>G