Canonical Allele Identifier: PA2825804574
Gene: MYOT HGNC NCBI

Linked Data

ClinVar Variation Id: 167318
ClinVar RCV Id: RCV000323304 RCV000378013 RCV000723809 RCV001437646 RCV004019839
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001129412.1:p.Asp217Glu
CA234299
NM_001135940.2:c.651T>A
CA361056423
NM_001135940.2:c.651T>G