Canonical Allele Identifier: PA100869
Gene: C1QC HGNC NCBI

Linked Data

ClinVar Variation Id: 17071

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107573.1:p.Gly34Arg
CA677888
NM_001114101.1:c.100G>A
CA338932982
NM_001114101.1:c.100G>C