Canonical Allele Identifier: PA2828569432
Gene: CFI HGNC NCBI

Linked Data

ClinVar Variation Id: 438686
ClinVar RCV Id: RCV000505641 RCV001865643 RCV002490847
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001362213.1:p.Ser367Thr
CA3041835
NM_001375284.1:c.1100G>C