Canonical Allele Identifier: PA658670727
Gene: MYOT HGNC NCBI

Linked Data

ClinVar Variation Id: 464372
ClinVar RCV Id: RCV000536530

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006781.1:p.Ala131Ser
CA361053985
NM_006790.3:c.391G>T