Canonical Allele Identifier: PA2828083299
Gene: CFAP418 HGNC NCBI

Linked Data

ClinVar Variation Id: 522286
ClinVar RCV Id: RCV000625263 RCV001167827 RCV001700418 RCV003889939 RCV003905669
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350189.1:p.Asn90Ser
CA4815197
NM_001363260.1:c.269A>G