Canonical Allele Identifier: PA916035753
Gene: DYM HGNC NCBI

Linked Data

ClinVar Variation Id: 161709
ClinVar RCV Id: RCV000149245

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340143.1:p.Ile593Met
CA174639
NM_001353214.3:c.1779C>G