Canonical Allele Identifier: PA2828736470
Gene: CCDC78 HGNC NCBI

Linked Data

ClinVar Variation Id: 540481
ClinVar RCV Id: RCV000650527 RCV003945651
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001364962.1:p.Arg159Gln
CA7789300
NM_001378033.1:c.476G>A