Allele Registry

Canonical Allele Identifier: PA916037864

Gene: C1R HGNC NCBI

ClinVar RCV:

RCV000412507

RCV000755111

ClinVar Variation:

372129

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341275.1:p.Gly311Asp	CA16042208 NM_001354346.2:c.932G>A