Canonical Allele Identifier: PA645430238
Gene: WDR35 HGNC NCBI

Linked Data

ClinVar Variation Id: 437865
ClinVar RCV Id: RCV000504572
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001006658.1:p.Arg472Gln
CA1543248
NM_001006657.2:c.1415G>A