Canonical Allele Identifier: PA658676876
Gene: CCDC78 HGNC NCBI

Linked Data

ClinVar Variation Id: 447011

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001026907.2:p.Ala325Pro
CA7789312
NM_001031737.3:c.973G>C