Canonical Allele Identifier: PA2826915424
Gene: AUH HGNC NCBI

Linked Data

ClinVar Variation Id: 214153

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001293119.1:p.Ile127Met
CA324949
NM_001306190.2:c.381A>G