Canonical Allele Identifier: PA916037864
Gene: C1R HGNC NCBI

Linked Data

ClinVar Variation Id: 372129

Amino-acid Alleles

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