Canonical Allele Identifier: PA2828736466
Gene: CCDC78 HGNC NCBI

Linked Data

ClinVar Variation Id: 2131802
ClinVar RCV Id: RCV003052538
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001364962.1:p.Ser157Asn
CA394098775
NM_001378033.1:c.470G>A