Canonical Allele Identifier: PA174532
Gene: MYOT HGNC NCBI

Linked Data

ClinVar Variation Id: 161651
ClinVar RCV Id: RCV000149187
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006781.1:p.Ser229Ile
CA174530
NM_006790.3:c.686G>T