Canonical Allele Identifier: PA2573074619
Gene: CCDC78 HGNC NCBI

Linked Data

ClinVar Variation Id: 540481

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001364959.1:p.Arg348Gln
CA7789300
NM_001378030.1:c.1043G>A