Canonical Allele Identifier: PA2828569408
Gene: CFI HGNC NCBI
ClinVar Allele:
27161
ClinVar RCV:
RCV000012905
ClinVar Variation:
12122
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001362213.1:p.Asp321Val
CA256214
NM_001375284.1:c.962A>T