Canonical Allele Identifier: PA2827021589
Gene: CNPY3 HGNC NCBI

Linked Data

ClinVar Variation Id: 518429
ClinVar RCV Id: RCV000615970

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305771.1:p.Gly158Arg
CA364183152
NM_001318842.1:c.472G>C