Canonical Allele Identifier: PA2741876015
Gene: CCDC78 HGNC NCBI

Linked Data

ClinVar Variation Id: 2865926
ClinVar RCV Id: RCV003648626
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001364959.1:p.Leu359Val
CA276519709
NM_001378030.1:c.1075C>G