Canonical Allele Identifier: PA2829955480
Gene: WDR35 HGNC NCBI

Linked Data

ClinVar Variation Id: 471482
ClinVar RCV Id: RCV000593049 RCV000552845 RCV001141933 RCV001570965 RCV001141934 RCV004538037
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065830.2:p.Ile416Met
CA1543288
NM_020779.4:c.1248T>G