Canonical Allele Identifier: PA915965460
Gene: CFH HGNC NCBI

Linked Data

ClinVar Variation Id: 636910
ClinVar RCV Id: RCV000788876 RCV003453633 RCV003456146 RCV003453632 RCV003453631
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000177.2:p.Gly1194Asp
CA1305983
NM_000186.4:c.3581G>A