Canonical Allele Identifier: PA2829955728
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_065830.2:p.Trp1142Cys
CA346230640
NM_020779.4:c.3426G>C
CA346230642
NM_020779.4:c.3426G>T