Canonical Allele Identifier: PA257492
Gene: CFH HGNC NCBI

Linked Data

ClinVar Variation Id: 16542
ClinVar RCV Id: RCV000018008 RCV001328244
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000177.2:p.Arg1215Gly
CA257490
NM_000186.4:c.3643C>G