Canonical Allele Identifier: PA645389489
Gene: CFHR5 HGNC NCBI

Linked Data

ClinVar Variation Id: 294536

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_110414.1:p.Val110Ala
CA1307697
NM_030787.4:c.329T>C