Canonical Allele Identifier: PA645453859
Gene: MYOT HGNC NCBI

Linked Data

ClinVar Variation Id: 351025
ClinVar RCV Id: RCV000347504 RCV000386833 RCV000874867 RCV001557068 RCV000594719 RCV002523507 RCV003950243
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006781.1:p.Arg178His
CA3422946
NM_006790.3:c.533G>A