Canonical Allele Identifier: PA2741825193
Gene: CFH HGNC NCBI

Linked Data

ClinVar Variation Id: 2910128
ClinVar RCV Id: RCV003734559
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001014975.1:p.Val144Met
CA1305065
NM_001014975.3:c.430G>A