Canonical Allele Identifier: PA2826520779
Gene: CFAP410 HGNC NCBI

Linked Data

ClinVar Variation Id: 942624
ClinVar RCV Id: RCV001212646
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001258370.1:p.Trp93Arg
CA410456764
NM_001271441.2:c.277T>A
CA410456765
NM_001271441.2:c.277T>C