Canonical Allele Identifier: PA2826915392
Gene: AUH HGNC NCBI

Linked Data

ClinVar Variation Id: 1219237
ClinVar RCV Id: RCV001588326 RCV002070456 RCV002592499 RCV003931237
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001293119.1:p.Pro47Leu
CA5119953
NM_001306190.2:c.140C>T