Canonical Allele Identifier: PA2829906859
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_062830.1:p.Asp1298Gly
CA8874020
NM_019856.2:c.3893A>G