Canonical Allele Identifier: PA645430201
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_001006658.1:p.Arg119Cys
CA1543553
NM_001006657.2:c.355C>T