Canonical Allele Identifier: PA2830054152
Gene: WDR19 HGNC NCBI

Linked Data

ClinVar Variation Id: 1523876
ClinVar RCV Id: RCV002031297
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_079408.3:p.Leu225Ile
CA356633972
NM_025132.4:c.673C>A