Canonical Allele Identifier: PA2826855657
Gene: MYOT HGNC NCBI

Linked Data

ClinVar Variation Id: 288959
ClinVar RCV Id: RCV000295763 RCV000335309 RCV000402251 RCV000639970 RCV003417907 RCV003323496
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001287840.1:p.Ala314Gly
CA3423144
NM_001300911.2:c.941C>G