Canonical Allele Identifier: PA2826972553
Gene: WDR19 HGNC NCBI

Linked Data

ClinVar Variation Id: 266105
ClinVar RCV Id: RCV000256446 RCV000985142
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001304853.1:p.Ile318Met
CA10588960
NM_001317924.2:c.954C>G