Canonical Allele Identifier: PA2829955693
Gene: WDR35 HGNC NCBI
ClinVar RCV:
RCV001878650
ClinVar Variation:
1358516
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065830.2:p.Thr1009Ile
CA345941650
NM_020779.4:c.3026C>T