Canonical Allele Identifier: PA2825354591
Gene: CCDC78 HGNC NCBI

Linked Data

ClinVar Variation Id: 1491006
ClinVar RCV Id: RCV001986215
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001026907.2:p.Gln351Arg
CA7789299
NM_001031737.3:c.1052A>G