Canonical Allele Identifier: PA645425225
Gene: CFH HGNC NCBI

Linked Data

ClinVar Variation Id: 294511
ClinVar RCV Id: RCV000260915 RCV000315933 RCV000375168 RCV000388064 RCV000835731 RCV002294235 RCV001849179 RCV004537633 RCV003987498
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000177.2:p.Thr956Met
CA1305764
NM_000186.4:c.2867C>T