Canonical Allele Identifier: PA128915
Gene: AUH HGNC NCBI

Linked Data

ClinVar Variation Id: 30079
ClinVar RCV Id: RCV000022982 RCV000196605
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001689.1:p.Gly187Ser
CA128913
NM_001698.3:c.559G>A