Canonical Allele Identifier: PA915956948
Gene: CP HGNC NCBI

Linked Data

ClinVar Variation Id: 434819
ClinVar RCV Id: RCV000503433 RCV004023365
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000087.2:p.Asp654Asn
CA2660871
NM_000096.4:c.1960G>A