Canonical Allele Identifier: PA2830054142
Gene: WDR19 HGNC NCBI

Linked Data

ClinVar Variation Id: 1976984
ClinVar RCV Id: RCV002736410
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_079408.3:p.Ile202Val
CA356633698
NM_025132.4:c.604A>G