Canonical Allele Identifier: PA2828514941
Gene: DYM HGNC NCBI

Linked Data

ClinVar Variation Id: 191094
ClinVar RCV Id: RCV000171274

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361363.1:p.Ser141Asn
CA236000
NM_001374434.1:c.422G>A