Canonical Allele Identifier: PA2580198567
Gene: WDR19 HGNC NCBI

Linked Data

ClinVar Variation Id: 1924598
ClinVar RCV Id: RCV002634870
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001304853.1:p.Thr50Ala
CA95686083
NM_001317924.2:c.148A>G