Canonical Allele Identifier: PA645430287
Gene: WDR35 HGNC NCBI

Linked Data

ClinVar Variation Id: 333377

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001006658.1:p.Leu904Ser
CA1542859
NM_001006657.2:c.2711T>C