Canonical Allele Identifier: PA2829955520
Gene: WDR35 HGNC NCBI

Linked Data

ClinVar Variation Id: 333393
ClinVar RCV Id: RCV000273395 RCV000878115 RCV000312074 RCV001574327
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065830.2:p.Leu531Val
CA1543169
NM_020779.4:c.1591C>G