Canonical Allele Identifier: PA354902
Gene: MSMO1 HGNC NCBI

Linked Data

ClinVar Variation Id: 222974
ClinVar RCV Id: RCV000208581
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006736.1:p.His173Gln
CA354901
NM_006745.5:c.519T>A
CA358686141
NM_006745.5:c.519T>G