Canonical Allele Identifier: PA2580240456
Gene: CCDC78 HGNC NCBI

Linked Data

ClinVar Variation Id: 2131802
ClinVar RCV Id: RCV003052538
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001364959.1:p.Ser346Asn
CA394098775
NM_001378030.1:c.1037G>A