Canonical Allele Identifier: PA2825581223
Gene: WDR26 HGNC NCBI

Linked Data

ClinVar Variation Id: 522069
ClinVar RCV Id: RCV000623249

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001108585.2:p.Cys640Phe
CA344722552
NM_001115113.3:c.1919G>T