Canonical Allele Identifier: PA2573220207
Gene: CFB HGNC NCBI

Linked Data

ClinVar Variation Id: 1383679
ClinVar RCV Id: RCV001892784
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001701.2:p.Ser83Gly
CA363389407
NM_001710.6:c.247A>G