Canonical Allele Identifier: PA645380318
Gene: CCDC39 HGNC NCBI

Linked Data

ClinVar Variation Id: 344276
ClinVar RCV Id: RCV000385217 RCV002429307
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_852091.1:p.Gly274Glu
CA2716073
NM_181426.2:c.821G>A