Allele Registry

Canonical Allele Identifier: PA916037865

Gene: C1R HGNC NCBI

ClinVar RCV:

RCV000258067

RCV000755112

ClinVar Variation:

267354

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341275.1:p.Leu314Pro	CA16040617 NM_001354346.2:c.941T>C