Allele Registry

Canonical Allele Identifier: PA340467

Gene: MYOT HGNC NCBI

ClinVar Allele:

20873

ClinVar RCV:

RCV000424803

RCV000639976

ClinVar Variation:

5834

HGVS (amino-acid)	Matching Registered Transcripts
NP_006781.1:p.Thr57Ile	CA340465 NM_006790.3:c.170C>T