Canonical Allele Identifier: PA2825282717
Gene: WDR35 HGNC NCBI
ClinVar RCV:
RCV001243953
ClinVar Variation:
968745
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001006658.1:p.Thr1001Ala
CA345941769
NM_001006657.2:c.3001A>G