Canonical Allele Identifier: PA916037859
Gene: C1R HGNC NCBI

Linked Data

ClinVar Variation Id: 372130
ClinVar RCV Id: RCV000412647 RCV000755109
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341275.1:p.Val64Asp
CA16042209
NM_001354346.2:c.191_192delinsAT
CA383729756
NM_001354346.2:c.191T>A