Canonical Allele Identifier: PA915956867
Gene: CP HGNC NCBI

Linked Data

ClinVar Variation Id: 42120
ClinVar RCV Id: RCV000034947
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000087.2:p.Gln165Glu
CA344570
NM_000096.4:c.493C>G