Canonical Allele Identifier: PA2580102268
Gene: CP HGNC NCBI

Linked Data

ClinVar Variation Id: 2061890
ClinVar RCV Id: RCV002939158
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000087.2:p.Ala653_Asp654del
CA2660868
NM_000096.4:c.1958_1963del