Canonical Allele Identifier: PA355729
Gene: CCDC39 HGNC NCBI

Linked Data

ClinVar Variation Id: 220134
ClinVar RCV Id: RCV000205312 RCV000765714
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_852091.1:p.Asn686Ser
CA349473
NM_181426.2:c.2057A>G