Canonical Allele Identifier: PA230973
Gene: CCDC78 HGNC NCBI

Linked Data

ClinVar Variation Id: 128634
ClinVar RCV Id: RCV000116606 RCV001082148
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001026907.2:p.Asn322Lys
CA230972
NM_001031737.3:c.966C>A
CA394099158
NM_001031737.3:c.966C>G