Canonical Allele Identifier: PA2580316672
Gene: OMD HGNC NCBI

Linked Data

ClinVar Variation Id: 2284408
ClinVar RCV Id: RCV004138487
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005005.1:p.Ser246Tyr
CA5124499
NM_005014.3:c.737C>A