Canonical Allele Identifier: PA645380328
Gene: CCDC39 HGNC NCBI

Linked Data

ClinVar Variation Id: 262977
ClinVar RCV Id: RCV000246808 RCV000370071 RCV001094894
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_852091.1:p.His300Gln
CA2716059
NM_181426.2:c.900T>A
CA355300295
NM_181426.2:c.900T>G