Canonical Allele Identifier: PA259803
Gene: MYOT HGNC NCBI

Linked Data

ClinVar Variation Id: 30407
ClinVar RCV Id: RCV000023360 RCV001588824
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006781.1:p.Arg6His
CA259801
NM_006790.3:c.17G>A