Canonical Allele Identifier: PA126186
Gene: CFB HGNC NCBI

Linked Data

ClinVar Variation Id: 16077
ClinVar RCV Id: RCV000017457 RCV000264554 RCV000288622 RCV000385220 RCV000454952 RCV001516300 RCV001154195 RCV002490378 RCV004549374
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001701.2:p.Leu9His
CA126184
NM_001710.6:c.26T>A