Canonical Allele Identifier: PA2741876012
Gene: CCDC78 HGNC NCBI

Linked Data

ClinVar Variation Id: 2715056
ClinVar RCV Id: RCV003534136
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001364959.1:p.Arg348Trp
CA7789303
NM_001378030.1:c.1042C>T