Canonical Allele Identifier: PA658676805
Gene: CCDC78 HGNC NCBI

Linked Data

ClinVar Variation Id: 473259
ClinVar RCV Id: RCV000537626 RCV003156257
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001026907.2:p.Asn156Lys
CA7789585
NM_001031737.3:c.468T>G
CA394103163
NM_001031737.3:c.468T>A