Canonical Allele Identifier: PA2825772313
Gene: HYOU1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2190332
ClinVar RCV Id: RCV002612179
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124463.1:p.Ala324Val
CA229623537
NM_001130991.3:c.971C>T