Canonical Allele Identifier: PA2573076422
Gene: WDR26 HGNC NCBI

Linked Data

ClinVar Variation Id: 522069
ClinVar RCV Id: RCV000623249

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001366332.1:p.Cys756Phe
CA344722552
NM_001379403.1:c.2267G>T