Canonical Allele Identifier: PA112747
Gene: WDR35 HGNC NCBI

Linked Data

ClinVar Variation Id: 21
ClinVar RCV Id: RCV000000038
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001006658.1:p.Glu626Gly
CA339780
NM_001006657.2:c.1877A>G