Canonical Allele Identifier: PA105879
Gene: CFAP418 HGNC NCBI

Linked Data

ClinVar Variation Id: 31194
ClinVar RCV Id: RCV000024193 RCV000477682 RCV001257837 RCV001002908 RCV002228055
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_808880.1:p.Arg177Trp
CA260013
NM_177965.3:c.529C>T