Canonical Allele Identifier: PA2829955619
Gene: WDR35 HGNC NCBI
ClinVar RCV:
RCV000516006
ClinVar Variation:
446645
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065830.2:p.Asp830Val
CA345942957
NM_020779.4:c.2489A>T