Canonical Allele Identifier: PA645501750
Gene: WDR19 HGNC NCBI

Linked Data

ClinVar Variation Id: 423393
ClinVar RCV Id: RCV000486591 RCV001078579 RCV001146438 RCV001821402 RCV001146437 RCV004535530
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_079408.3:p.Asp870Asn
CA2892126
NM_025132.4:c.2608G>A