Canonical Allele Identifier: PA2829955713
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_065830.2:p.Gln1093His
CA1542706
NM_020779.4:c.3279G>C
CA346231401
NM_020779.4:c.3279G>T