Canonical Allele Identifier: PA915956973
Gene: CP HGNC NCBI

Linked Data

ClinVar Variation Id: 217866
ClinVar RCV Id: RCV000201933
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000087.2:p.His997Gln
CA347691
NM_000096.4:c.2991T>G
CA354929147
NM_000096.4:c.2991T>A