Canonical Allele Identifier: PA915956970
Gene: CP HGNC NCBI

Linked Data

ClinVar Variation Id: 431113
ClinVar RCV Id: RCV000496150 RCV003226310
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000087.2:p.Leu919Pro
CA354929700
NM_000096.4:c.2756T>C