Canonical Allele Identifier: PA645481269
Gene: CCDC50 HGNC NCBI

Linked Data

ClinVar Variation Id: 228478
ClinVar RCV Id: RCV000214906

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_848018.1:p.Glu182Asp
CA2755279
NM_178335.3:c.546G>C
CA355763919
NM_178335.3:c.546G>T