Canonical Allele Identifier: PA658678255
Gene: MYOM1 HGNC NCBI

Linked Data

ClinVar Variation Id: 454453
ClinVar RCV Id: RCV000550232
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003794.3:p.Asp1394Gly
CA8874020
NM_003803.4:c.4181A>G