Canonical Allele Identifier: PA658673531
Gene: WDR19 HGNC NCBI

Linked Data

ClinVar Variation Id: 446637
ClinVar RCV Id: RCV000515949
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_079408.3:p.Asp159Asn
CA356632420
NM_025132.4:c.475G>A