Canonical Allele Identifier: PA199264
Gene: WDR19 HGNC NCBI
ClinVar RCV:
RCV000169776
ClinVar Variation:
189379
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_079408.3:p.Val68Asp
CA199263
NM_025132.4:c.203T>A