Canonical Allele Identifier: PA2828736471
Gene: CCDC78 HGNC NCBI

Linked Data

ClinVar Variation Id: 1001168
ClinVar RCV Id: RCV001297422
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001364962.1:p.Arg159Leu
CA394098733
NM_001378033.1:c.476G>T