Canonical Allele Identifier: PA915956878
Gene: CP HGNC NCBI

Linked Data

ClinVar Variation Id: 42119
ClinVar RCV Id: RCV000034946
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000087.2:p.Pro196Arg
CA344568
NM_000096.4:c.587C>G