Canonical Allele Identifier: PA658808984
Gene: CFAP44 HGNC NCBI
ClinVar RCV:
RCV000626424
ClinVar Variation:
523151
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157968.1:p.Leu590Gln
CA2544063
NM_001164496.2:c.1769T>A