Canonical Allele Identifier: PA1139731490
Gene: WDR35 HGNC NCBI

Linked Data

ClinVar Variation Id: 968745
ClinVar RCV Id: RCV001243953
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065830.2:p.Thr990Ala
CA345941769
NM_020779.4:c.2968A>G