Canonical Allele Identifier: PA2827609601
Gene: AUH HGNC NCBI

Linked Data

ClinVar Variation Id: 976619

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338361.1:p.Ala118Thr
CA5119756
NM_001351432.2:c.352G>A