Canonical Allele Identifier: PA1139675199
Gene: WDR35 HGNC NCBI

Linked Data

ClinVar Variation Id: 838113
ClinVar RCV Id: RCV001039598 RCV002051911 RCV002551451
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001006658.1:p.Arg990Gln
CA1542800
NM_001006657.2:c.2969G>A