Canonical Allele Identifier: PA916037874
Gene: C1R HGNC NCBI

Linked Data

ClinVar Variation Id: 375579
ClinVar RCV Id: RCV000417050 RCV000755119
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341275.1:p.Trp378Cys
CA16044361
NM_001354346.2:c.1134G>C
CA2617391396
NM_001354346.2:c.1134G>T