Canonical Allele Identifier: PA658673535
Gene: WDR19 HGNC NCBI
ClinVar RCV:
RCV000515976
ClinVar Variation:
446640
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_079408.3:p.Phe249Ser
CA356634279
NM_025132.4:c.746T>C