Canonical Allele Identifier: PA645380322
Gene: CCDC39 HGNC NCBI

Linked Data

ClinVar Variation Id: 344275
ClinVar RCV Id: RCV000325833 RCV001094896
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_852091.1:p.Arg288His
CA2716066
NM_181426.2:c.863G>A