Canonical Allele Identifier: PA916050546
Gene: WDR35 HGNC NCBI

Linked Data

ClinVar Variation Id: 497211
ClinVar RCV Id: RCV000592980 RCV001139419 RCV001139418 RCV001370744 RCV004543315
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065830.2:p.Pro351Ala
CA1543357
NM_020779.4:c.1051C>G