Canonical Allele Identifier: PA324471
Gene: AUH HGNC NCBI

Linked Data

ClinVar Variation Id: 214145

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001689.1:p.Arg226Cys
CA324469
NM_001698.3:c.676C>T