Canonical Allele Identifier: PA915956943
Gene: CP HGNC NCBI
ClinVar RCV:
RCV000034880
ClinVar Variation:
42052
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000087.2:p.Gly625Glu
CA344483
NM_000096.4:c.1874G>A