Canonical Allele Identifier: PA2826972565
Gene: WDR19 HGNC NCBI

Linked Data

ClinVar Variation Id: 446641
ClinVar RCV Id: RCV000516069 RCV001316218
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001304853.1:p.Gly335Arg
CA356631901
NM_001317924.2:c.1003G>C