Canonical Allele Identifier: PA2826915447
Gene: AUH HGNC NCBI

Linked Data

ClinVar Variation Id: 1979155
ClinVar RCV Id: RCV002766115
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001293119.1:p.Arg197His
CA5119757
NM_001306190.2:c.590G>A