Canonical Allele Identifier: PA2829955736
Gene: WDR35 HGNC NCBI

Linked Data

ClinVar Variation Id: 288788
ClinVar RCV Id: RCV000377253 RCV001086217 RCV004535416
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065830.2:p.Ile1156Arg
CA1542655
NM_020779.4:c.3467T>G