Canonical Allele Identifier: PA658692028
Gene: WDR35 HGNC NCBI

Linked Data

ClinVar Variation Id: 488657
ClinVar RCV Id: RCV000578479
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001006658.1:p.Trp1153Cys
CA346230640
NM_001006657.2:c.3459G>C
CA346230642
NM_001006657.2:c.3459G>T