Canonical Allele Identifier: PA2580198570
Gene: WDR19 HGNC NCBI

Linked Data

ClinVar Variation Id: 2063630
ClinVar RCV Id: RCV002948607
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001304853.1:p.Asn57Ser
CA356633881
NM_001317924.2:c.170A>G