Canonical Allele Identifier: PA2828736451
Gene: CCDC78 HGNC NCBI

Linked Data

ClinVar Variation Id: 447011
ClinVar RCV Id: RCV000516842 RCV000650516
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001364962.1:p.Ala136Pro
CA7789312
NM_001378033.1:c.406G>C