Canonical Allele Identifier: PA2573254632
Gene: MYOT HGNC NCBI

Linked Data

ClinVar Variation Id: 1391939
ClinVar RCV Id: RCV001911119
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006781.1:p.Cys17Tyr
CA361477845
NM_006790.3:c.50G>A