Canonical Allele Identifier: PA916050551
Gene: WDR35 HGNC NCBI

Linked Data

ClinVar Variation Id: 288569
ClinVar RCV Id: RCV000515966 RCV000395590 RCV001143732 RCV001143733 RCV001086026 RCV002278315
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065830.2:p.Asn395Tyr
CA1543330
NM_020779.4:c.1183A>T