Canonical Allele Identifier: PA645430246
Gene: WDR35 HGNC NCBI

Linked Data

ClinVar Variation Id: 333393

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001006658.1:p.Leu542Val
CA1543169
NM_001006657.2:c.1624C>G