Canonical Allele Identifier: PA915956918
Gene: CP HGNC NCBI

Linked Data

ClinVar Variation Id: 343778
ClinVar RCV Id: RCV000271781 RCV001821042
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000087.2:p.Asn315Ser
CA2661191
NM_000096.4:c.944A>G