Canonical Allele Identifier: PA2827718384
Gene: DYM HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340141.1:p.Cys596Arg
CA116051
NM_001353212.3:c.1786T>C