Canonical Allele Identifier: PA2741885694
Gene: CFB HGNC NCBI

Linked Data

ClinVar Variation Id: 2775570
ClinVar RCV Id: RCV003661125

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001701.2:p.Gln616His
CA3728466
NM_001710.6:c.1848G>C
CA363410214
NM_001710.6:c.1848G>T