Canonical Allele Identifier: PA658814880
Gene: WDR26 HGNC NCBI

Linked Data

ClinVar Variation Id: 522069
ClinVar RCV Id: RCV000623249

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_079436.4:p.Cys656Phe
CA344722552
NM_025160.7:c.1967G>T