Canonical Allele Identifier: PA355743
Gene: CCDC39 HGNC NCBI

Linked Data

ClinVar Variation Id: 219718
ClinVar RCV Id: RCV000205337 RCV002485338 RCV003430762
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_852091.1:p.Thr850Ala
CA349495
NM_181426.2:c.2548A>G