Canonical Allele Identifier: PA2580453162
Gene: CCDC86 HGNC NCBI
ClinVar RCV:
RCV004152699
ClinVar Variation:
2304105
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077003.1:p.Thr204Ala
CA222805285
NM_024098.4:c.610A>G