Canonical Allele Identifier: PA916022111
Gene: WDR19 HGNC NCBI
ClinVar RCV:
RCV000515976
ClinVar Variation:
446640
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001304853.1:p.Phe89Ser
CA356634279
NM_001317924.2:c.266T>C