Canonical Allele Identifier: PA2826915460
Gene: AUH HGNC NCBI

Linked Data

ClinVar Variation Id: 214146

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001293119.1:p.Asp215Asn
CA320067
NM_001306190.2:c.643G>A