Canonical Allele Identifier: PA645385677
Gene: CFAP418 HGNC NCBI

Linked Data

ClinVar Variation Id: 283430
ClinVar RCV Id: RCV000265472 RCV000376242 RCV000400757 RCV001174660
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_808880.1:p.Lys174Arg
CA4815119
NM_177965.3:c.521A>G