Canonical Allele Identifier: PA658681898
Gene: CCDC39 HGNC NCBI

Linked Data

ClinVar Variation Id: 455021
ClinVar RCV Id: RCV001145559 RCV000537244
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_852091.1:p.Arg853His
CA2715642
NM_181426.2:c.2558G>A