Canonical Allele Identifier: PA101243
Gene: DYM HGNC NCBI

Linked Data

ClinVar Variation Id: 3189
ClinVar RCV Id: RCV000003340 RCV002512700
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060123.3:p.Glu87Lys
CA116050
NM_017653.6:c.259G>A