Canonical Allele Identifier: PA2499274915
Gene: MYOT HGNC NCBI

Linked Data

ClinVar Variation Id: 1025934
ClinVar RCV Id: RCV001326319
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006781.1:p.Pro23Thr
CA3422841
NM_006790.3:c.67C>A