Canonical Allele Identifier: PA915958257
Gene: CFAP69 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001034795.2:p.Gln876Arg
CA4333868
NM_001039706.3:c.2627A>G