ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA126662
Gene: CFH
HGNC
NCBI
Linked Data
ClinVar Variation Id:
16550
ClinVar RCV Id:
RCV000018017
RCV000190297
RCV000274380
RCV000374816
RCV000331871
RCV001579191
RCV002293982
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000177.2:p.Val62Ile
CA126660
NM_000186.4:c.184G>A