Canonical Allele Identifier: PA112736
Gene: WDR35 HGNC NCBI

Linked Data

ClinVar Variation Id: 23
ClinVar RCV Id: RCV000000040 RCV000508347
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001006658.1:p.Ala875Thr
CA339782
NM_001006657.2:c.2623G>A