Canonical Allele Identifier: PA2573198560
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_001304853.1:p.Leu65Ile
CA356633972
NM_001317924.2:c.193C>A