Canonical Allele Identifier: PA658800034
Gene: WDR35 HGNC NCBI

Linked Data

ClinVar Variation Id: 497213
ClinVar RCV Id: RCV000591516 RCV001137179 RCV001351694 RCV001137180 RCV004543316
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001006658.1:p.Val358Ile
CA1543350
NM_001006657.2:c.1072G>A