Canonical Allele Identifier: PA2825354570
Gene: CCDC78 HGNC NCBI

Linked Data

ClinVar Variation Id: 1350786
ClinVar RCV Id: RCV002042129
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001026907.2:p.Val339Leu
CA394098895
NM_001031737.3:c.1015G>T
CA394098897
NM_001031737.3:c.1015G>C