Canonical Allele Identifier: PA2829955694
Gene: WDR35 HGNC NCBI
ClinVar RCV:
RCV002301348
ClinVar Variation:
1715591
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065830.2:p.Ala1012Pro
CA345941633
NM_020779.4:c.3034G>C