Canonical Allele Identifier: PA207960
Gene: WDR35 HGNC NCBI

Linked Data

ClinVar Variation Id: 212590
ClinVar RCV Id: RCV000194057 RCV000648352 RCV001143632 RCV001143633 RCV001582689 RCV004530150
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001006658.1:p.Arg700His
CA207959
NM_001006657.2:c.2099G>A