Canonical Allele Identifier: PA2826915434
Gene: AUH HGNC NCBI

Linked Data

ClinVar Variation Id: 30079

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001293119.1:p.Gly158Ser
CA128913
NM_001306190.2:c.472G>A