Canonical Allele Identifier: PA2828083323
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_001350189.1:p.Lys142Arg
CA4815119
NM_001363260.1:c.425A>G