Canonical Allele Identifier: PA645430333
Gene: WDR35 HGNC NCBI

Linked Data

ClinVar Variation Id: 288788

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001006658.1:p.Ile1167Arg
CA1542655
NM_001006657.2:c.3500T>G