Canonical Allele Identifier: PA645430322
Gene: WDR35 HGNC NCBI

Linked Data

ClinVar Variation Id: 333369
ClinVar RCV Id: RCV000311978 RCV000945632 RCV000405190 RCV002278514 RCV004530345 RCV001660692
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001006658.1:p.Gln1104His
CA1542706
NM_001006657.2:c.3312G>C
CA346231401
NM_001006657.2:c.3312G>T