Allele Registry

Canonical Allele Identifier: PA117798

Gene: MYOT HGNC NCBI

ClinVar RCV:

RCV000516381

RCV002512824

ClinVar Variation:

5839

HGVS (amino-acid)	Matching Registered Transcripts
NP_006781.1:p.Ser39Phe	CA117796 NM_006790.3:c.116C>T