Canonical Allele Identifier: PA2826915450
Gene: AUH HGNC NCBI

Linked Data

ClinVar Variation Id: 976619
ClinVar RCV Id: RCV001253975 RCV002570550
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001293119.1:p.Ala198Thr
CA5119756
NM_001306190.2:c.592G>A