Canonical Allele Identifier: PA2828736472
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_001364962.1:p.Gln162Arg
CA7789299
NM_001378033.1:c.485A>G