Canonical Allele Identifier: PA2742022277
Gene: CCDC50 HGNC NCBI

Linked Data

ClinVar Variation Id: 2964551
ClinVar RCV Id: RCV003828173

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_848018.1:p.Asn215Asp
CA2755298
NM_178335.3:c.643A>G