Canonical Allele Identifier: PA2828083328
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_001350189.1:p.Gln150Arg
CA129739
NM_001363260.1:c.449A>G