Canonical Allele Identifier: PA1139699094
Gene: WDR19 HGNC NCBI

Linked Data

ClinVar Variation Id: 899609
ClinVar RCV Id: RCV001144280 RCV001150372 RCV001202820 RCV002480532 RCV002276635 RCV004528395
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001304853.1:p.Asp70Ala
CA2891675
NM_001317924.2:c.209A>C