Canonical Allele Identifier: PA2580127703
Gene: WDR35 HGNC NCBI
ClinVar RCV:
RCV002301348
ClinVar Variation:
1715591
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001006658.1:p.Ala1023Pro
CA345941633
NM_001006657.2:c.3067G>C