Canonical Allele Identifier: PA2580198576
Gene: WDR19 HGNC NCBI

Linked Data

ClinVar Variation Id: 1965438
ClinVar RCV Id: RCV002726814
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001304853.1:p.Asn73Asp
CA2891676
NM_001317924.2:c.217A>G