Canonical Allele Identifier: PA916019051
Gene: MYOT HGNC NCBI

Linked Data

ClinVar Variation Id: 464372
ClinVar RCV Id: RCV000536530

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001287840.1:p.Ala16Ser
CA361053985
NM_001300911.2:c.46G>T