Canonical Allele Identifier: PA2573164292
Gene: CFH HGNC NCBI

Linked Data

ClinVar Variation Id: 1423628

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000177.2:p.Val552Leu
CA1305453
NM_000186.4:c.1654G>C
CA343983576
NM_000186.4:c.1654G>T