Canonical Allele Identifier: PA915977776
Gene: MYOT HGNC NCBI

Linked Data

ClinVar Variation Id: 161651
ClinVar RCV Id: RCV000149187
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001129412.1:p.Ser45Ile
CA174530
NM_001135940.2:c.134G>T