Canonical Allele Identifier: PA645509835
Gene: WDR35 HGNC NCBI

Linked Data

ClinVar Variation Id: 440416
ClinVar RCV Id: RCV000508424 RCV000964762 RCV004541590
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001006658.1:p.Lys1123Arg
CA1542695
NM_001006657.2:c.3368A>G