Canonical Allele Identifier: PA891864420
Gene: C1R HGNC NCBI

Linked Data

ClinVar Variation Id: 375580
ClinVar RCV Id: RCV000417063 RCV000755120
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001724.4:p.Cys371Trp
CA16044360
NM_001733.7:c.1113C>G