Canonical Allele Identifier: PA2825939352
Gene: CFAP69 HGNC NCBI
ClinVar RCV:
RCV000938573
ClinVar Variation:
760606
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153610.1:p.Gln858Arg
CA4333868
NM_001160138.2:c.2573A>G