Canonical Allele Identifier: PA658800785
Gene: CCDC78 HGNC NCBI

Linked Data

ClinVar Variation Id: 540468
ClinVar RCV Id: RCV000650511 RCV002531962
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001026907.2:p.Arg179Gln
CA7789543
NM_001031737.3:c.536G>A