Canonical Allele Identifier: PA2573176075
Gene: WDR35 HGNC NCBI
ClinVar RCV:
RCV001938275
ClinVar Variation:
1417308
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001006658.1:p.Ile978Thr
CA1542811
NM_001006657.2:c.2933T>C