Canonical Allele Identifier: PA2830044578
Gene: CCNP HGNC NCBI

Linked Data

ClinVar Variation Id: 3139990
ClinVar RCV Id: RCV004430814
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_079153.2:p.Gly51Asp
CA9441312
NM_024877.4:c.152G>A