Canonical Allele Identifier: PA916029112
Gene: C1QC HGNC NCBI

Linked Data

ClinVar Variation Id: 440743
ClinVar RCV Id: RCV000508986 RCV003546567 RCV003221355
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001334549.1:p.Gly75Ser
CA677990
NM_001347620.2:c.223G>A