Canonical Allele Identifier: PA2573100399
Gene: CCDC50 HGNC NCBI

Linked Data

ClinVar Variation Id: 1313640
ClinVar RCV Id: RCV001764004

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_848018.1:p.Gly174Arg
CA355763791
NM_178335.3:c.520G>C
CA355763793
NM_178335.3:c.520G>A