Canonical Allele Identifier: PA105887
Gene: CFAP418 HGNC NCBI

Linked Data

ClinVar Variation Id: 31195
ClinVar RCV Id: RCV000024194 RCV001002907
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_808880.1:p.Gln182Arg
CA129739
NM_177965.3:c.545A>G