Allele Registry

Canonical Allele Identifier: PA253628

Gene: MYOT HGNC NCBI

ClinVar RCV:

RCV000006195

ClinVar Variation:

5838

HGVS (amino-acid)	Matching Registered Transcripts
NP_006781.1:p.Ser95Ile	CA253626 NM_006790.3:c.284G>T