Allele Registry

Canonical Allele Identifier: PA259803

Gene: MYOT HGNC NCBI

ClinVar RCV:

RCV000023360

RCV001588824

ClinVar Variation:

30407

HGVS (amino-acid)	Matching Registered Transcripts
NP_006781.1:p.Arg6His	CA259801 NM_006790.3:c.17G>A