Canonical Allele Identifier: PA1139764790
Gene: CCDC39 HGNC NCBI

Linked Data

ClinVar Variation Id: 942739
ClinVar RCV Id: RCV001212776
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_852091.1:p.Glu222del
CA1056965832
NM_181426.2:c.664_666del