Canonical Allele Identifier: PA2826521173
Gene: CFAP410 HGNC NCBI

Linked Data

ClinVar Variation Id: 1412601
ClinVar RCV Id: RCV001919140
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001258371.1:p.Pro46Leu
CA10053748
NM_001271442.1:c.137C>T