Canonical Allele Identifier: PA2826586486
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_001265224.1:p.Val126Met
CA2116352
NM_001278295.1:c.376G>A