Canonical Allele Identifier: PA2573287368
Gene: WDR19 HGNC NCBI

Linked Data

ClinVar Variation Id: 1389139
ClinVar RCV Id: RCV001887010 RCV003434343
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_079408.3:p.Arg878Cys
CA2892129
NM_025132.4:c.2632C>T