Canonical Allele Identifier: PA658806924
Gene: CCDC39 HGNC NCBI

Linked Data

ClinVar Variation Id: 525559
ClinVar RCV Id: RCV000629636 RCV003640930
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_852091.1:p.Gln91Arg
CA2716208
NM_181426.2:c.272A>G