Canonical Allele Identifier: PA324951
Gene: AUH HGNC NCBI

Linked Data

ClinVar Variation Id: 214153
ClinVar RCV Id: RCV000275240 RCV000487826
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001689.1:p.Ile127Met
CA324949
NM_001698.3:c.381A>G