Canonical Allele Identifier: PA645430231
Gene: WDR35 HGNC NCBI

Linked Data

ClinVar Variation Id: 288569
ClinVar RCV Id: RCV000515966 RCV000395590 RCV001143732 RCV001143733 RCV001086026 RCV002278315
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001006658.1:p.Asn395Tyr
CA1543330
NM_001006657.2:c.1183A>T