Canonical Allele Identifier: PA344944
Gene: WDR35 HGNC NCBI

Linked Data

ClinVar Variation Id: 65620
ClinVar RCV Id: RCV000055831
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001006658.1:p.Leu531Pro
CA344943
NM_001006657.2:c.1592T>C