Canonical Allele Identifier: PA2826647276
Gene: C2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2025905
ClinVar RCV Id: RCV002880655
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269386.1:p.Pro10His
CA363496075
NM_001282457.2:c.29C>A