Allele Registry

Canonical Allele Identifier: PA658670711

Gene: MYOT HGNC NCBI

ClinVar RCV:

RCV000615351

RCV000712368

RCV001079228

ClinVar Variation:

464369

HGVS (amino-acid)	Matching Registered Transcripts
NP_006781.1:p.Gln74Lys	CA128097466 NM_006790.3:c.220C>A