Canonical Allele Identifier: PA658676877
Gene: CCDC78 HGNC NCBI

Linked Data

ClinVar Variation Id: 473246
ClinVar RCV Id: RCV000550251
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001026907.2:p.His347Tyr
CA7789304
NM_001031737.3:c.1039C>T