Canonical Allele Identifier: PA2828085859
Gene: CFAP69 HGNC NCBI
ClinVar RCV:
RCV000938573
ClinVar Variation:
760606
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350367.1:p.Gln810Arg
CA4333868
NM_001363438.1:c.2429A>G