Canonical Allele Identifier: PA2741813057
Gene: CFH HGNC NCBI

Linked Data

ClinVar Variation Id: 2570747
ClinVar RCV Id: RCV003312148

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000177.2:p.Pro1226Ser
CA343989405
NM_000186.4:c.3676C>T