Canonical Allele Identifier: PA146987
Gene: WDR35 HGNC NCBI

Linked Data

ClinVar Variation Id: 93463
ClinVar RCV Id: RCV000079360 RCV000279775 RCV000375441 RCV000545999 RCV001711226
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001006658.1:p.Val867Phe
CA146986
NM_001006657.2:c.2599G>T