Canonical Allele Identifier: PA2826586538
Gene: CFAP65 HGNC NCBI

Linked Data

ClinVar Variation Id: 2226527
ClinVar RCV Id: RCV004091160
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265225.1:p.Pro584Leu
CA2115811
NM_001278296.2:c.1751C>T