Canonical Allele Identifier: PA916050542
Gene: WDR35 HGNC NCBI

Linked Data

ClinVar Variation Id: 446644
ClinVar RCV Id: RCV000516065 RCV000755748 RCV000608080 RCV001353118 RCV001764511 RCV000578486 RCV000851218
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065830.2:p.Trp311Leu
CA1543388
NM_020779.4:c.932G>T