Canonical Allele Identifier: PA2741819738
Gene: CR1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2600161
ClinVar RCV Id: RCV004345608
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000642.3:p.Ser189Ala
CA344519923
NM_000651.6:c.565T>G