Canonical Allele Identifier: PA2829955657
Gene: WDR35 HGNC NCBI

Linked Data

ClinVar Variation Id: 195803
ClinVar RCV Id: RCV000176461 RCV000266710 RCV000363678 RCV001078877 RCV004539638
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065830.2:p.Tyr926Cys
CA242420
NM_020779.4:c.2777A>G