Canonical Allele Identifier: PA2827719063
Gene: DYM HGNC NCBI

Linked Data

ClinVar Variation Id: 191094
ClinVar RCV Id: RCV000171274

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340145.1:p.Ser141Asn
CA236000
NM_001353216.3:c.422G>A