Canonical Allele Identifier: PA2825199492
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_000564.2:p.Ser189Ala
CA344519923
NM_000573.4:c.565T>G