Canonical Allele Identifier: PA320902
Gene: AUH HGNC NCBI

Linked Data

ClinVar Variation Id: 214149

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001689.1:p.Ala275Val
CA320900
NM_001698.3:c.824C>T