Canonical Allele Identifier: PA915956968
Gene: CP HGNC NCBI

Linked Data

ClinVar Variation Id: 42054
ClinVar RCV Id: RCV000034882 RCV000334692 RCV000419016 RCV001836633
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000087.2:p.Gly895Ala
CA152494
NM_000096.4:c.2684G>C