Canonical Allele Identifier: PA2580146062
Gene: CFAP96 HGNC NCBI

Linked Data

ClinVar Variation Id: 2373634
ClinVar RCV Id: RCV004553916
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107829.1:p.Glu285Lys
CA3158879
NM_001114357.3:c.853G>A