Canonical Allele Identifier: PA916056550
Gene: CFHR3 HGNC NCBI

Linked Data

ClinVar Variation Id: 778240
ClinVar RCV Id: RCV000958850 RCV001702753
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066303.2:p.Pro241Ser
CA1306258
NM_021023.5:c.721C>T