Allele Registry

Canonical Allele Identifier: PA658676888

Gene: CCDC78 HGNC NCBI

ClinVar Allele:

465947

ClinVar RCV:

RCV000538424

ClinVar Variation:

473250

HGVS (amino-acid)	Matching Registered Transcripts
NP_001026907.2:p.Gly404Arg	CA7789117 NM_001031737.3:c.1210G>A CA394097828 NM_001031737.3:c.1210G>C