Canonical Allele Identifier: PA658676798
Gene: CCDC78 HGNC NCBI

Linked Data

ClinVar Variation Id: 473258
ClinVar RCV Id: RCV000544640 RCV004024231
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001026907.2:p.Arg123Gln
CA7789636
NM_001031737.3:c.368G>A