Canonical Allele Identifier: PA2580520770
Gene: CFAP65 HGNC NCBI

Linked Data

ClinVar Variation Id: 2398216
ClinVar RCV Id: RCV004226916
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_689602.2:p.Val72Met
CA2116352
NM_152389.4:c.214G>A