Canonical Allele Identifier: PA645509833
Gene: WDR35 HGNC NCBI

Linked Data

ClinVar Variation Id: 440412
ClinVar RCV Id: RCV000507380 RCV000578488 RCV001266500
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001006658.1:p.Tyr1068Cys
CA1542728
NM_001006657.2:c.3203A>G