Canonical Allele Identifier: PA2826972885
Gene: WDR19 HGNC NCBI

Linked Data

ClinVar Variation Id: 1522585
ClinVar RCV Id: RCV002036121
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001304853.1:p.Lys1011Asn
CA2892404
NM_001317924.2:c.3033A>T
CA356647283
NM_001317924.2:c.3033A>C