Canonical Allele Identifier: PA645453854
Gene: MYOT HGNC NCBI

Linked Data

ClinVar Variation Id: 351023
ClinVar RCV Id: RCV000317621 RCV000372249 RCV000598161 RCV000875382 RCV002523506
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006781.1:p.Ala115Ser
CA3422885
NM_006790.3:c.343G>T