Canonical Allele Identifier: PA2741885686
Gene: CFB HGNC NCBI

Linked Data

ClinVar Variation Id: 2786971
ClinVar RCV Id: RCV003660481
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001701.2:p.Glu549Asp
CA3728423
NM_001710.6:c.1647G>T
CA363408651
NM_001710.6:c.1647G>C