Canonical Allele Identifier: PA915956885
Gene: CP HGNC NCBI

Linked Data

ClinVar Variation Id: 42051
ClinVar RCV Id: RCV000034879
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000087.2:p.Phe217Ser
CA344481
NM_000096.4:c.650T>C