Canonical Allele Identifier: PA658681886
Gene: CCDC39 HGNC NCBI

Linked Data

ClinVar Variation Id: 455026
ClinVar RCV Id: RCV000525221
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_852091.1:p.Thr230Ile
CA355302063
NM_181426.2:c.689C>T