Canonical Allele Identifier: PA645414059
Gene: CR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 402559
ClinVar RCV Id: RCV000455065 RCV001653784 RCV001521613
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001006659.1:p.Ser639Asn
CA1368823
NM_001006658.3:c.1916G>A