Canonical Allele Identifier: PA1139704190
Gene: CFB HGNC NCBI

Linked Data

ClinVar Variation Id: 906097

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001701.2:p.Thr92Ser
CA3727973
NM_001710.6:c.274A>T
CA363389749
NM_001710.6:c.275C>G