Allele Registry

Canonical Allele Identifier: PA253622

Gene: MYOT HGNC NCBI

ClinVar RCV:

RCV000006193

RCV000239643

RCV000725007

ClinVar Variation:

5836

HGVS (amino-acid)	Matching Registered Transcripts
NP_006781.1:p.Ser60Cys	CA253620 NM_006790.3:c.179C>G