Canonical Allele Identifier: PA2829955647
Gene: WDR35 HGNC NCBI

Linked Data

ClinVar Variation Id: 333377
ClinVar RCV Id: RCV000324159 RCV000358005 RCV000733656 RCV001480464 RCV004544616
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065830.2:p.Leu893Ser
CA1542859
NM_020779.4:c.2678T>C