Canonical Allele Identifier: PA915956858
Gene: CP HGNC NCBI

Linked Data

ClinVar Variation Id: 128843
ClinVar RCV Id: RCV000116823 RCV001087501 RCV003925135
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000087.2:p.His108Tyr
CA231058
NM_000096.4:c.322C>T