Canonical Allele Identifier: PA2829955518
Gene: WDR35 HGNC NCBI

Linked Data

ClinVar Variation Id: 65620
ClinVar RCV Id: RCV000055831

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065830.2:p.Leu520Pro
CA344943
NM_020779.4:c.1559T>C