Canonical Allele Identifier: PA2829955677
Gene: WDR35 HGNC NCBI
ClinVar RCV:
RCV001938275
ClinVar Variation:
1417308
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065830.2:p.Ile967Thr
CA1542811
NM_020779.4:c.2900T>C