Canonical Allele Identifier: PA658817362
Gene: CNPY3 HGNC NCBI

Linked Data

ClinVar Variation Id: 518429
ClinVar RCV Id: RCV000615970
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006577.2:p.Gly125Arg
CA364183152
NM_006586.5:c.373G>C