Canonical Allele Identifier: PA915956940
Gene: CP HGNC NCBI

Linked Data

ClinVar Variation Id: 424620
ClinVar RCV Id: RCV000487430
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000087.2:p.Cys560Phe
CA16621520
NM_000096.4:c.1679G>T