Canonical Allele Identifier: PA915956929
Gene: CP HGNC NCBI

Linked Data

ClinVar Variation Id: 343773
ClinVar RCV Id: RCV000260851 RCV001770276 RCV002520097
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000087.2:p.Ala406Glu
CA2661092
NM_000096.4:c.1217C>A