Canonical Allele Identifier: PA2499291536
Gene: WDR19 HGNC NCBI

Linked Data

ClinVar Variation Id: 1022968
ClinVar RCV Id: RCV001322947
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_079408.3:p.Met1170Val
CA2892403
NM_025132.4:c.3508A>G