Canonical Allele Identifier: PA2828736476
Gene: CCDC78 HGNC NCBI

Linked Data

ClinVar Variation Id: 1349222
ClinVar RCV Id: RCV002051003

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001364962.1:p.Gly164Ser
CA7789271
NM_001378033.1:c.490G>A