Canonical Allele Identifier: PA915956963
Gene: CP HGNC NCBI

Linked Data

ClinVar Variation Id: 343753
ClinVar RCV Id: RCV000364282 RCV000514945 RCV003912452
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000087.2:p.Asp871Asn
CA2660675
NM_000096.4:c.2611G>A