Allele Registry

Canonical Allele Identifier: PA645453854

Gene: MYOT HGNC NCBI

ClinVar RCV:

RCV000317621

RCV000372249

RCV000598161

RCV000875382

RCV002523506

ClinVar Variation:

351023

HGVS (amino-acid)	Matching Registered Transcripts
NP_006781.1:p.Ala115Ser	CA3422885 NM_006790.3:c.343G>T