Canonical Allele Identifier: PA658673538
Gene: WDR19 HGNC NCBI

Linked Data

ClinVar Variation Id: 446635
ClinVar RCV Id: RCV000516052 RCV001851417
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_079408.3:p.Gly294Arg
CA2891724
NM_025132.4:c.880G>A
CA356634568
NM_025132.4:c.880G>C