Canonical Allele Identifier: PA2827609560
Gene: AUH HGNC NCBI

Linked Data

ClinVar Variation Id: 214153

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338361.1:p.Ile18Met
CA324949
NM_001351432.2:c.54A>G