Canonical Allele Identifier: PA645430197
Gene: WDR35 HGNC NCBI

Linked Data

ClinVar Variation Id: 333407
ClinVar RCV Id: RCV000294691 RCV000291625 RCV000391047 RCV000607352 RCV001139538 RCV001139539 RCV001522540
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001006658.1:p.Gln18Arg
CA1543648
NM_001006657.2:c.53A>G