Canonical Allele Identifier: PA2827719168
Gene: DYM HGNC NCBI

Linked Data

ClinVar Variation Id: 1500997
ClinVar RCV Id: RCV002017137
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340145.1:p.Asn497Asp
CA300365732
NM_001353216.3:c.1489A>G