Canonical Allele Identifier: PA916031054
Gene: AUH HGNC NCBI

Linked Data

ClinVar Variation Id: 30079

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338362.1:p.Gly78Ser
CA128913
NM_001351433.2:c.232G>A