Canonical Allele Identifier: PA2827609532
Gene: AUH HGNC NCBI

Linked Data

ClinVar Variation Id: 214149
ClinVar RCV Id: RCV000196487 RCV000624471 RCV001853168
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338360.1:p.Ala166Val
CA320900
NM_001351431.2:c.497C>T