Allele Registry

Canonical Allele Identifier: PA2827718471

Gene: DYM HGNC NCBI

ClinVar RCV:

RCV000171274

ClinVar Variation:

191094

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340142.1:p.Ser141Asn	CA236000 NM_001353213.3:c.422G>A