Canonical Allele Identifier: PA2826915385
Gene: AUH HGNC NCBI

Linked Data

ClinVar Variation Id: 136474
ClinVar RCV Id: RCV000123791 RCV000326682 RCV000676897
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001293119.1:p.Cys26Tyr
CA289616
NM_001306190.2:c.77G>A