Canonical Allele Identifier: PA2829955565
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_065830.2:p.Arg689His
CA207959
NM_020779.4:c.2066G>A