Canonical Allele Identifier: PA2827719193
Gene: DYM HGNC NCBI

Linked Data

ClinVar Variation Id: 326889

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340145.1:p.Val569Met
CA8957911
NM_001353216.3:c.1705G>A