Canonical Allele Identifier: PA658661939
Gene: WDR35 HGNC NCBI

Linked Data

ClinVar Variation Id: 431796
ClinVar RCV Id: RCV000515824 RCV000591001 RCV003326443
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001006658.1:p.Gly69Asp
CA43388469
NM_001006657.2:c.206G>A