ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA915958257
Gene: CFAP69
HGNC
NCBI
Linked Data
ClinVar RCV:
RCV000938573
ClinVar Variation:
760606
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001034795.2:p.Gln876Arg
CA4333868
NM_001039706.3:c.2627A>G