Canonical Allele Identifier: PA2828083325
Gene: CFAP418 HGNC NCBI

Linked Data

ClinVar Variation Id: 31194
ClinVar RCV Id: RCV000024193 RCV000477682 RCV001257837 RCV001002908 RCV002228055
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350189.1:p.Arg145Trp
CA260013
NM_001363260.1:c.433C>T