Canonical Allele Identifier: PA2580548808
Gene: CFAP65 HGNC NCBI

Linked Data

ClinVar Variation Id: 2212423
ClinVar RCV Id: RCV004081986
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_919278.2:p.Ala1648Thr
CA2114782
NM_194302.4:c.4942G>A