Canonical Allele Identifier: PA658661953
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_001006658.1:p.Ile427Met
CA1543288
NM_001006657.2:c.1281T>G