Canonical Allele Identifier: PA2741993362
Gene: CFHR5 HGNC NCBI

Linked Data

ClinVar Variation Id: 2514771
ClinVar RCV Id: RCV003248699
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_110414.1:p.Arg223Ser
CA1307832
NM_030787.4:c.669A>C
CA344004688
NM_030787.4:c.669A>T