Canonical Allele Identifier: PA103106
Gene: WDR11 HGNC NCBI

Linked Data

ClinVar Variation Id: 68842
ClinVar RCV Id: RCV000059801 RCV000988456 RCV002287360
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060587.8:p.Phe1150Leu
CA220082
NM_018117.12:c.3450T>G
CA378317126
NM_018117.12:c.3448T>C
CA378317142
NM_018117.12:c.3450T>A