Canonical Allele Identifier: PA2827718371
Gene: DYM HGNC NCBI

Linked Data

ClinVar Variation Id: 1500997
ClinVar RCV Id: RCV002017137

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340141.1:p.Asn551Asp
CA300365732
NM_001353212.3:c.1651A>G