Canonical Allele Identifier: PA916050519
Gene: WDR35 HGNC NCBI

Linked Data

ClinVar Variation Id: 281109
ClinVar RCV Id: RCV000280618 RCV000356360 RCV000375021 RCV001085930 RCV000767100 RCV004535250
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065830.2:p.Arg119Cys
CA1543553
NM_020779.4:c.355C>T