Canonical Allele Identifier: PA2829955636
Gene: WDR35 HGNC NCBI

Linked Data

ClinVar Variation Id: 23

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065830.2:p.Ala864Thr
CA339782
NM_020779.4:c.2590G>A